Hart Lidov

Dissecting the immune landscape in pediatric high-grade glioma reveals cell state changes under therapeutic pressure. Cell Rep Med. 2025 May 20; 6(5):102095. View Dissecting the immune landscape in pediatric high-grade glioma reveals cell state changes under therapeutic pressure. Abstract

Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. Brain Commun. 2025; 7(2):fcaf113. View Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. Abstract

Systemically injected oxygen within rapidly dissolving microbubbles improves the outcomes of severe hypoxaemia in swine. Nat Biomed Eng. 2024 11; 8(11):1396-1411. View Systemically injected oxygen within rapidly dissolving microbubbles improves the outcomes of severe hypoxaemia in swine. Abstract

The choroid plexus synergizes with immune cells during neuroinflammation. Cell. 2024 Sep 05; 187(18):4946-4963.e17. View The choroid plexus synergizes with immune cells during neuroinflammation. Abstract

Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy. Muscle Nerve. 2024 Oct; 70(4):843-850. View Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy. Abstract

Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. medRxiv. 2024 Jul 22. View Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. Abstract

Clinical utility of DNA methylation profiling for choroid plexus tumors. Neurooncol Adv. 2024 Jan-Dec; 6(1):vdae097. View Clinical utility of DNA methylation profiling for choroid plexus tumors. Abstract

H3K27-altered diffuse midline gliomas with MAPK pathway alterations: Prognostic and therapeutic implications. J Neuropathol Exp Neurol. 2023 12 22; 83(1):30-35. View H3K27-altered diffuse midline gliomas with MAPK pathway alterations: Prognostic and therapeutic implications. Abstract

Somatic Mosaicism in PIK3CA Variant Correlates With Stereoelectroencephalography-Derived Electrophysiology. Neurol Genet. 2024 Feb; 10(1):e200117. View Somatic Mosaicism in PIK3CA Variant Correlates With Stereoelectroencephalography-Derived Electrophysiology. Abstract

Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy. Nat Genet. 2023 Nov; 55(11):1920-1928. View Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy. Abstract

Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy. N Engl J Med. 2023 09 28; 389(13):1203-1210. View Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy. Abstract

Non-vascular intracranial lesions in three children with PHACE association. Pediatr Dermatol. 2024 Mar-Apr; 41(2):284-288. View Non-vascular intracranial lesions in three children with PHACE association. Abstract

A collaboration between immune cells and the choroid plexus epithelium in brain inflammation. bioRxiv. 2023 Aug 08. View A collaboration between immune cells and the choroid plexus epithelium in brain inflammation. Abstract

Variants in DTNA cause a mild, dominantly inherited muscular dystrophy. Acta Neuropathol. 2023 04; 145(4):479-496. View Variants in DTNA cause a mild, dominantly inherited muscular dystrophy. Abstract

Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings. Ophthalmic Genet. 2023 Dec; 44(6):598-601. View Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings. Abstract

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene. Neurology. 2023 01 31; 100(5):e528-e542. View Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene. Abstract

PD-L1 and PD-1 expression in pediatric central nervous system germ cell tumors. Mod Pathol. 2022 12; 35(12):1770-1774. View PD-L1 and PD-1 expression in pediatric central nervous system germ cell tumors. Abstract

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations. Brain. 2022 08 27; 145(8):2704-2720. View Somatic variants in diverse genes leads to a spectrum of focal cortical malformations. Abstract

Disruption of GMNC-MCIDAS multiciliogenesis program is critical in choroid plexus carcinoma development. Cell Death Differ. 2022 08; 29(8):1596-1610. View Disruption of GMNC-MCIDAS multiciliogenesis program is critical in choroid plexus carcinoma development. Abstract

"Spokes of Wheel" in Muscle Biopsy. J Clin Neuromuscul Dis. 2022 Mar 01; 23(3):160-161. View "Spokes of Wheel" in Muscle Biopsy. Abstract

Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. Am J Med Genet A. 2022 03; 188(3):907-910. View Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. Abstract

Spatiotemporal changes in diffusivity and anisotropy in fetal brain tractography. Hum Brain Mapp. 2021 12 01; 42(17):5771-5784. View Spatiotemporal changes in diffusivity and anisotropy in fetal brain tractography. Abstract

Medulloblastoma in the setting of megalencephaly polymicrogyria polydactyly hydrocephalus. Am J Med Genet A. 2021 05; 185(5):1614-1618. View Medulloblastoma in the setting of megalencephaly polymicrogyria polydactyly hydrocephalus. Abstract

Loss of histone H3 trimethylation on lysine 27 and nuclear expression of transducin-like enhancer 1 in primary intracranial sarcoma, DICER1-mutant. Histopathology. 2021 Jan; 78(2):265-275. View Loss of histone H3 trimethylation on lysine 27 and nuclear expression of transducin-like enhancer 1 in primary intracranial sarcoma, DICER1-mutant. Abstract

Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile. Mod Pathol. 2021 02; 34(2):264-279. View Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile. Abstract

A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability. Eur J Med Genet. 2020 Apr; 63(4):103826. View A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability. Abstract

Increasing value of autopsies in patients with brain tumors in the molecular era. J Neurooncol. 2019 Nov; 145(2):349-355. View Increasing value of autopsies in patients with brain tumors in the molecular era. Abstract

White matter mean diffusivity correlates with myelination in tuberous sclerosis complex. Ann Clin Transl Neurol. 2019 07; 6(7):1178-1190. View White matter mean diffusivity correlates with myelination in tuberous sclerosis complex. Abstract

Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in Swine. JACC Basic Transl Sci. 2019 Apr; 4(2):176-187. View Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in Swine. Abstract

Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites. Mol Genet Genomic Med. 2019 03; 7(3):e552. View Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites. Abstract

Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System. J Neuropathol Exp Neurol. 2018 12 01; 77(12):1079-1084. View Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System. Abstract

The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Rep. 2018 07 24; 24(4):973-986.e8. View The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Abstract

PHOX2B is a reliable immunomarker in distinguishing peripheral neuroblastic tumours from CNS embryonal tumours. Histopathology. 2018 Sep; 73(3):483-491. View PHOX2B is a reliable immunomarker in distinguishing peripheral neuroblastic tumours from CNS embryonal tumours. Abstract

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Ann Neurol. 2018 06; 83(6):1133-1146. View Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Abstract

Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors. Am J Pathol. 2018 06; 188(6):1334-1344. View Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors. Abstract

Multiparametric Analysis of Permeability and ADC Histogram Metrics for Classification of Pediatric Brain Tumors by Tumor Grade. AJNR Am J Neuroradiol. 2018 Mar; 39(3):552-557. View Multiparametric Analysis of Permeability and ADC Histogram Metrics for Classification of Pediatric Brain Tumors by Tumor Grade. Abstract

A novel GIT2-BRAF fusion in pilocytic astrocytoma. Diagn Pathol. 2017 Nov 15; 12(1):82. View A novel GIT2-BRAF fusion in pilocytic astrocytoma. Abstract

Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors. Neuro Oncol. 2017 Jul 01; 19(7):986-996. View Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors. Abstract

GM2 Activator Deficiency Caused by a Homozygous Exon 2 Deletion in GM2A. JIMD Rep. 2018; 38:61-65. View GM2 Activator Deficiency Caused by a Homozygous Exon 2 Deletion in GM2A. Abstract

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant. Cold Spring Harb Mol Case Stud. 2017 03; 3(2):a001560. View AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant. Abstract

The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States. J Hum Genet. 2017 Feb; 62(2):243-252. View The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States. Abstract

Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations. Sci Rep. 2016 05 20; 6:26202. View Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations. Abstract

Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-a protein (PMPCA) cause a severe mitochondrial disease. Cold Spring Harb Mol Case Stud. 2016 May; 2(3):a000786. View Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-a protein (PMPCA) cause a severe mitochondrial disease. Abstract

Sonic Hedgehog promotes proliferation of Notch-dependent monociliated choroid plexus tumour cells. Nat Cell Biol. 2016 Apr; 18(4):418-30. View Sonic Hedgehog promotes proliferation of Notch-dependent monociliated choroid plexus tumour cells. Abstract

EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy. Brain. 2016 Mar; 139(Pt 3):765-81. View EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy. Abstract

Tubers are neither static nor discrete: Evidence from serial diffusion tensor imaging. Neurology. 2015 Nov 03; 85(18):1536-45. View Tubers are neither static nor discrete: Evidence from serial diffusion tensor imaging. Abstract

Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia. J Exp Med. 2015 Jun 01; 212(6):939-51. View Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia. Abstract

Spatially heterogeneous choroid plexus transcriptomes encode positional identity and contribute to regional CSF production. J Neurosci. 2015 Mar 25; 35(12):4903-16. View Spatially heterogeneous choroid plexus transcriptomes encode positional identity and contribute to regional CSF production. Abstract

Rasmussen's encephalitis presenting as focal cortical dysplasia. Epilepsy Behav Case Rep. 2014; 2:86-9. View Rasmussen's encephalitis presenting as focal cortical dysplasia. Abstract

Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas. Nat Genet. 2014 Feb; 46(2):161-5. View Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas. Abstract

The lost art of localization: Franc Ingraham's legacy in pediatric neurosurgery. J Neurosurg Pediatr. 2013 Dec; 12(6):642-54. View The lost art of localization: Franc Ingraham's legacy in pediatric neurosurgery. Abstract

Intrasacral meningocele in the pediatric population. J Neurosurg Pediatr. 2013 Jun; 11(6):615-22. View Intrasacral meningocele in the pediatric population. Abstract

OTX2 represses myogenic and neuronal differentiation in medulloblastoma cells. Cancer Res. 2012 Nov 15; 72(22):5988-6001. View OTX2 represses myogenic and neuronal differentiation in medulloblastoma cells. Abstract

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores. Neurogenetics. 2012 May; 13(2):115-24. View Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores. Abstract

Primary calcified rhabdoid meningioma of the cranio-cervical junction: A case report and review of literature. J Craniovertebr Junction Spine. 2012 Jan; 3(1):32-7. View Primary calcified rhabdoid meningioma of the cranio-cervical junction: A case report and review of literature. Abstract

Rapid reversal of uremic neuropathy following renal transplantation in an adolescent. Pediatr Transplant. 2012 Nov; 16(7):E296-300. View Rapid reversal of uremic neuropathy following renal transplantation in an adolescent. Abstract

Extradural en-plaque spinal meningioma with intraneural invasion. World Neurosurg. 2012 Jan; 77(1):202.e5-13. View Extradural en-plaque spinal meningioma with intraneural invasion. Abstract

Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. BMC Med Genet. 2011 Jun 28; 12:87. View Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. Abstract

Pediatric sciatic neuropathy associated with neoplasms. Muscle Nerve. 2011 Feb; 43(2):183-8. View Pediatric sciatic neuropathy associated with neoplasms. Abstract

Hypothermic circulatory arrest increases permeability of the blood brain barrier in watershed areas. Ann Thorac Surg. 2010 Dec; 90(6):2001-8. View Hypothermic circulatory arrest increases permeability of the blood brain barrier in watershed areas. Abstract

Differential neuronal vulnerability varies according to specific cardiopulmonary bypass insult in a porcine survival model. J Thorac Cardiovasc Surg. 2010 Dec; 140(6):1408-15.e1-3. View Differential neuronal vulnerability varies according to specific cardiopulmonary bypass insult in a porcine survival model. Abstract

Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies. Hum Mol Genet. 2010 Oct 15; 19(20):3995-4006. View Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies. Abstract

Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene. Development. 2010 Aug; 137(16):2643-52. View Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene. Abstract

Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy. Muscle Nerve. 2010 Jun; 41(6):746-50. View Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy. Abstract

Optimal dose of aprotinin for neuroprotection and renal function in a piglet survival model. J Thorac Cardiovasc Surg. 2009 Jun; 137(6):1521-9; discussion 1529. View Optimal dose of aprotinin for neuroprotection and renal function in a piglet survival model. Abstract

Aprotinin protects the cerebral microcirculation during cardiopulmonary bypass. Perfusion. 2009 Mar; 24(2):99-105. View Aprotinin protects the cerebral microcirculation during cardiopulmonary bypass. Abstract

A case of congenital glycogen storage disease type IV with a novel GBE1 mutation. J Child Neurol. 2008 Mar; 23(3):349-52. View A case of congenital glycogen storage disease type IV with a novel GBE1 mutation. Abstract

Dystrophin,:the dystrophin associated protein complex, and muscular dystrophy. New Encyclopedia of Neuroscience, ed. Squire L., et..al. 2008.

Distinctive patterns of microRNA expression in primary muscular disorders. Proc Natl Acad Sci U S A. 2007 Oct 23; 104(43):17016-21. View Distinctive patterns of microRNA expression in primary muscular disorders. Abstract

Extracranial metastases of glioblastoma in a child: case report and review of the literature. J Pediatr Hematol Oncol. 2007 Mar; 29(3):190-4. View Extracranial metastases of glioblastoma in a child: case report and review of the literature. Abstract

The neuropathology of Vici syndrome. J Neuropathol Exp Neurol. 2007; 60:528.

Aprotinin improves cerebral protection: evidence from a survival porcine model. J Thorac Cardiovasc Surg. 2006 Oct; 132(4):948-53. View Aprotinin improves cerebral protection: evidence from a survival porcine model. Abstract

A novel mutation in two families with limb-girdle muscular dystrophy type 2C. Neurology. 2006 Jul 11; 67(1):167-9. View A novel mutation in two families with limb-girdle muscular dystrophy type 2C. Abstract

Specific bypass conditions determine safe minimum flow rate. Ann Thorac Surg. 2005 Oct; 80(4):1460-7. View Specific bypass conditions determine safe minimum flow rate. Abstract

Variations in gene expression among different types of human skeletal muscle. Muscle Nerve. 2005 Oct; 32(4):483-91. View Variations in gene expression among different types of human skeletal muscle. Abstract

Tissue oxygenation index is a useful monitor of histologic and neurologic outcome after cardiopulmonary bypass in piglets. J Thorac Cardiovasc Surg. 2005 Aug; 130(2):384-92. View Tissue oxygenation index is a useful monitor of histologic and neurologic outcome after cardiopulmonary bypass in piglets. Abstract

IKKbeta/NF-kappaB activation causes severe muscle wasting in mice. Cell. 2004 Oct 15; 119(2):285-98. View IKKbeta/NF-kappaB activation causes severe muscle wasting in mice. Abstract

Interaction of temperature with hematocrit level and pH determines safe duration of hypothermic circulatory arrest. J Thorac Cardiovasc Surg. 2004 Aug; 128(2):220-32. View Interaction of temperature with hematocrit level and pH determines safe duration of hypothermic circulatory arrest. Abstract

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Hum Mol Genet. 2004 Sep 15; 13(18):1999-2010. View Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Abstract

Higher bypass temperature correlates with increased white cell activation in the cerebral microcirculation. J Thorac Cardiovasc Surg. 2004 Jun; 127(6):1781-8. View Higher bypass temperature correlates with increased white cell activation in the cerebral microcirculation. Abstract

Skeletal muscle diseases. In: Gray F, DeGirolami U, Poirier J (eds.) Escourolle and Poirier Manual of BasicNeuropathology. 2004; 281-314.

Diagnostic value of electromyography and muscle biopsy in arthrogryposis multiplex congenita. Ann Neurol. 2003 Dec; 54(6):790-5. View Diagnostic value of electromyography and muscle biopsy in arthrogryposis multiplex congenita. Abstract

Cerebral amyloid angiopathy associated with primary angiitis of the central nervous system: report of 2 cases and review of the literature. Arthritis Rheum. 2003 Jun 15; 49(3):421-7. View Cerebral amyloid angiopathy associated with primary angiitis of the central nervous system: report of 2 cases and review of the literature. Abstract

Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle. Proc Natl Acad Sci U S A. 2003 Apr 15; 100(8):4666-71. View Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle. Abstract

Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation. J Clin Invest. 2002 Sep; 110(6):807-14. View Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation. Abstract

Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Neuromuscul Disord. 2002 Mar; 12(3):273-80. View Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Abstract

Combination of alpha-stat strategy and hemodilution exacerbates neurologic injury in a survival piglet model with deep hypothermic circulatory arrest. Ann Thorac Surg. 2002 Jan; 73(1):180-9; discussion 189-90. View Combination of alpha-stat strategy and hemodilution exacerbates neurologic injury in a survival piglet model with deep hypothermic circulatory arrest. Abstract

Prediction of safe duration of hypothermic circulatory arrest by near-infrared spectroscopy. J Thorac Cardiovasc Surg. 2001 Aug; 122(2):339-50. View Prediction of safe duration of hypothermic circulatory arrest by near-infrared spectroscopy. Abstract

Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin. Proc Natl Acad Sci U S A. 2001 May 22; 98(11):6156-61. View Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin. Abstract

Granulomatous angiitis with ƒÒ-amyloid angiopathy as a mass lesion. J Neuropathol Exp Neurol. 2001; 60:528.

Commentary. J Thorac Cardiovasc Surg. 2001; 121:968-970.

The molecular neuropathology of the muscular dystrophies: a review and update. J Neuropathol Exp Neurol. 2000 Dec; 59(12):1019-30. View The molecular neuropathology of the muscular dystrophies: a review and update. Abstract

Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein. J Cell Biol. 2000 Jan 10; 148(1):115-26. View Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein. Abstract

Gangliocytoma masquerading as a prolactinoma. Case report. J Neurosurg. 1999 Sep; 91(3):490-5. View Gangliocytoma masquerading as a prolactinoma. Case report. Abstract

Oxygenation strategy and neurologic damage after deep hypothermic circulatory arrest. II. hypoxic versus free radical injury. J Thorac Cardiovasc Surg. 1999 Jun; 117(6):1172-9. View Oxygenation strategy and neurologic damage after deep hypothermic circulatory arrest. II. hypoxic versus free radical injury. Abstract

A novel sialyl Lewis X analog attenuates cerebral injury after deep hypothermic circulatory arrest. J Thorac Cardiovasc Surg. 1999 Jun; 117(6):1204-11. View A novel sialyl Lewis X analog attenuates cerebral injury after deep hypothermic circulatory arrest. Abstract

Molecular organization of sarcoglycan complex in mouse myotubes in culture. J Cell Biol. 1998 Dec 28; 143(7):2033-44. View Molecular organization of sarcoglycan complex in mouse myotubes in culture. Abstract

Dystrophin and Dp140 in the adult rodent kidney. Lab Invest. 1998 Dec; 78(12):1543-51. View Dystrophin and Dp140 in the adult rodent kidney. Abstract

Postischemic hyperthermia exacerbates neurologic injury after deep hypothermic circulatory arrest. J Thorac Cardiovasc Surg. 1998 Nov; 116(5):780-92. View Postischemic hyperthermia exacerbates neurologic injury after deep hypothermic circulatory arrest. Abstract

Caveolin-3 in muscular dystrophy. Hum Mol Genet. 1998 May; 7(5):871-7. View Caveolin-3 in muscular dystrophy. Abstract

Effects of oncotic pressure and hematocrit on outcome after hypothermic circulatory arrest. Ann Thorac Surg. 1998 Jan; 65(1):155-64. View Effects of oncotic pressure and hematocrit on outcome after hypothermic circulatory arrest. Abstract

Immunocytochemistry in Limb-Girdle Dystrophy with identified sarcoglycan mutations. J Neuropathol Exp Neurol. 1998; 57:491.

Dp140: alternatively spliced isoforms in brain and kidney. Genomics. 1997 Oct 01; 45(1):132-9. View Dp140: alternatively spliced isoforms in brain and kidney. Abstract

Molecular characterization of Br-cadherin, a developmentally regulated, brain-specific cadherin. Proc Natl Acad Sci U S A. 1997 Mar 18; 94(6):2398-403. View Molecular characterization of Br-cadherin, a developmentally regulated, brain-specific cadherin. Abstract

Higher hematocrit improves cerebral outcome after deep hypothermic circulatory arrest. J Thorac Cardiovasc Surg. 1996 Dec; 112(6):1610-20; discussion 1620-1. View Higher hematocrit improves cerebral outcome after deep hypothermic circulatory arrest. Abstract

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. Am J Hum Genet. 1996 Nov; 59(5):1040-7. View Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. Abstract

Intermittent whole-body perfusion with "somatoplegia' versus blood perfusate to extend duration of circulatory arrest. Circulation. 1996 Nov 01; 94(9 Suppl):II56-62. View Intermittent whole-body perfusion with "somatoplegia' versus blood perfusate to extend duration of circulatory arrest. Abstract

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. Hum Mol Genet. 1996 Nov; 5(11):1841-7. View Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. Abstract

Dystrophin in the nervous system. Brain Pathol. 1996 Jan; 6(1):63-77. View Dystrophin in the nervous system. Abstract

The Neuropathology of a swine bypass model. J Neuropathol Exp Neurol. 1996; 55:666.

University of Wisconsin cerebroplegia in a piglet survival model of circulatory arrest. Ann Thorac Surg. 1995 Dec; 60(6 Suppl):S494-500. View University of Wisconsin cerebroplegia in a piglet survival model of circulatory arrest. Abstract

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus. Hum Mol Genet. 1995 Mar; 4(3):329-35. View Dp140: a novel 140 kDa CNS transcript from the dystrophin locus. Abstract

An alternative dystrophin transcript specific to peripheral nerve. Nat Genet. 1993 May; 4(1):77-81. View An alternative dystrophin transcript specific to peripheral nerve. Abstract

The distribution of dystrophin in the murine central nervous system: an immunocytochemical study. Neuroscience. 1993 May; 54(1):167-87. View The distribution of dystrophin in the murine central nervous system: an immunocytochemical study. Abstract

Dystrophin and Duchenne Muscular Dystrophy. In: Adelman G, Smith B. editors. Encyclopedia of Neuroscience. 1993; 1999.

The Zellweger-Adrenoleukodystrophy Spectrum: An Intermediate Case. J Neuropathol Exp Neurol. 1993; 52:298.

The distribution of dystrophin in the murine CNS: an immunocytochemical study. Neuropath Appl Neurol. 1993; 19:193-4.

Dystrophin and Duchenne Muscular Dystrophy. In: Adelman G, Smith B. editors. Neuroscience Year: Supplement. 1993; 45-8.

An Immunocytochemical study of 427kD dystrophin in the mouse CNS. J.Neurochem. 1993; Suppl 61:S234.

Dystrophin and Duchenne Muscular Dystrophy. In: Adelman G, Smith B. editors. Encyclopedia of Neuroscience. 1993; 594-9.

Neuroenteric cyst of the optic nerve: case report with immunohistochemical study. J Neurol Neurosurg Psychiatry. 1992 Dec; 55(12):1197-9. View Neuroenteric cyst of the optic nerve: case report with immunohistochemical study. Abstract

Cerebral neoplastic angioendotheleosis complicated by hypercalcaemia. Postgrad Med J. 1991 Jun; 67(788):571-3. View Cerebral neoplastic angioendotheleosis complicated by hypercalcaemia. Abstract

Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons. Nature. 1990 Dec 20-27; 348(6303):725-8. View Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons. Abstract

An ependymoma involving the pituitary fossa. J Neurol Neurosurg Psychiatry. 1989 Dec; 52(12):1443-4. View An ependymoma involving the pituitary fossa. Abstract

Progressive medullary failure associated with neurofibrillary degeneration. J Neurol Neurosurg Psychiatry. 1989 May; 52(5):643-7. View Progressive medullary failure associated with neurofibrillary degeneration. Abstract

Neuropathology of infants dying after extracorporeal membrane oxygenation (ECMO). J Neuropathol Exp Neurol. 1989; 48:307.

Antenatal sonographic diagnosis of cebocephaly. J Ultrasound Med. 1988 Jul; 7(7):395-8. View Antenatal sonographic diagnosis of cebocephaly. Abstract

Lhermitte-Duclos disease (dysplastic gangliocytoma): a case report with CT and MRI. Acta Neurochir (Wien). 1988; 93(3-4):149-53. View Lhermitte-Duclos disease (dysplastic gangliocytoma): a case report with CT and MRI. Abstract

Serotoninergic differentiation of quail neural crest cells in vitro. Dev Biol. 1983 Oct; 99(2):352-9. View Serotoninergic differentiation of quail neural crest cells in vitro. Abstract

Immunohistochemical study of the development of serotonergic neurons in the rat CNS. Brain Res Bull. 1982 Jul-Dec; 9(1-6):559-604. View Immunohistochemical study of the development of serotonergic neurons in the rat CNS. Abstract

Noradrenergic and serotonergic fibers innervate complementary layers in monkey primary visual cortex: an immunohistochemical study. Proc Natl Acad Sci U S A. 1982 Apr; 79(7):2401-5. View Noradrenergic and serotonergic fibers innervate complementary layers in monkey primary visual cortex: an immunohistochemical study. Abstract

An immunohistochemical study of serotonin neuron development in the rat: ascending pathways and terminal fields. Brain Res Bull. 1982 Apr; 8(4):389-430. View An immunohistochemical study of serotonin neuron development in the rat: ascending pathways and terminal fields. Abstract

The structure of cerebral cortex in the rat following prenatal administration of 6-hydroxydopamine. Brain Res. 1982 Jan; 255(1):81-108. View The structure of cerebral cortex in the rat following prenatal administration of 6-hydroxydopamine. Abstract

Monoamine systems in the cerebral cortex. In: Palay S, Chan-Palay V. editors. Cytochemical Methods in Neuroanatomy. 1982; 255-277.

The distribution and development of the monoaminergic afferents to immature rodent neocortex[dissertation]. 1981.

The serotonin innervation of the cerebral cortex in the rat--an immunohistochemical analysis. Neuroscience. 1980; 5(2):207-27. View The serotonin innervation of the cerebral cortex in the rat--an immunohistochemical analysis. Abstract

Complmentarity of dopaminergic and noradrenergic innervation in anterior cingulate cortex of the rat. Brain Res. 1979 Mar 23; 164:328-33. View Complmentarity of dopaminergic and noradrenergic innervation in anterior cingulate cortex of the rat. Abstract

Characterization of the monoaminergic innervation of immature rat neocortex: a histofluorescence analysis. J Comp Neurol. 1978 Oct 01; 181(3):663-79. View Characterization of the monoaminergic innervation of immature rat neocortex: a histofluorescence analysis. Abstract

The organization of the catecholamine innervation of somatosensory cortex: the barrel field of the mouse. Brain Res. 1978 Sep 29; 153(3):577-84. View The organization of the catecholamine innervation of somatosensory cortex: the barrel field of the mouse. Abstract