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Eli Sprecher, MD, MPP
Pediatrician, Children's Hospital Primary Care Center (CHPCC); Assistant Director, Value Based Care
Assistant Professor of Pediatrics, Harvard Medical School
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Eli Sprecher, MD, MPP
Pediatrician, Children's Hospital Primary Care Center (CHPCC); Assistant Director, Value Based Care
Assistant Professor of Pediatrics, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
Harvard College
2005
Cambridge
MA
Graduate School
Harvard Kennedy School of Government
2011
Cambridge
MA
Medical School
Mount Sinai School of Medicine
2011
New York
NY
Internship
Boston Combined Residency Program (BCRP)
2011
Boston
MA
Residency
Boston Combined Residency Program (BCRP)
2014
Boston
MA
Fellowship
General Academic Pediatric
Boston Children's Hospital
2017
Boston
MA
Certifications
American Board of Pediatrics (General)
Professional History
In addition to clinical practice, I work in improving systems of care for children.
Approach to Care
I strive to provide high-quality, evidence-based, equitable, whole-child care to all.
Publications
What makes an epidermal differentiation disorder syndromic? Work in progress. View Abstract
Improving Pediatric Concussion Management in the Primary Care Setting. View Abstract
Potent neutralization by antibodies targeting the MPXV A28 protein. View Abstract
Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia. View Abstract
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation. View Abstract
Proposing an immune-inclusive lens to the new epidermal differentiation disorders classification: reply from authors. View Abstract
New gene-based classification of ichthyoses and palmoplantar keratodermas: Hereditary epidermal differentiation disorders. View Abstract
Comment on 'A proposal for a new pathogenesis-guided classification for inherited epidermal differentiation disorders': reply from authors. View Abstract
Reduction in Dressing Change Burden in Patients With Epidermolysis Bullosa-Impact of Oleogel-S10. View Abstract
Child and Family Characteristics Associated With Age of Autism Spectrum Disorder Diagnosis in a Primary Care Population. View Abstract
The Importance of Shared Patient Voices in Advancing Science for Genodermatoses on a Global Scale. View Abstract
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients. View Abstract
Advances in Pemphigus and Pemphigoid: A Report of the International Meeting of the Pemphigus and Pemphigoid Foundation in Thessaloniki, Greece. View Abstract
"I'm His Voice": Parent Perspectives on Obtaining an Autism Diagnosis and Services and the Influence of Personal and Cultural Factors. View Abstract
Relationship among sleep, work features, and SARS-cov-2 vaccine antibody response in hospital workers. View Abstract
Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches. View Abstract
Improving Asthma Action Plan Completion Rates across Five Divisions in an Academic Children's Hospital. View Abstract
Impact of the COVID-19 Pandemic on Childhood Lead Testing and Blood Lead Levels. View Abstract
Categorization of a Universal Coding System to Distinguish Use of Durable Medical Equipment and Supplies in Pediatric Patients. View Abstract
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4. View Abstract
Corrigendum: S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV). View Abstract
S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV). View Abstract
Ichthyosis. View Abstract
A Mixed-Methods Assessment of Coronavirus Disease of 2019-Era Telehealth Acute Care Visits in the Medical Home. View Abstract
Monitoring oral propranolol for infantile hemangiomata. View Abstract
Randomized Controlled Trial of Health Coaching for Parents of Children With Medical Complexity. View Abstract
Machine learning approaches to predicting no-shows in pediatric medical appointment. View Abstract
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti-tumour necrosis factor-a and interleukin-12/23 blockade. View Abstract
How Do Experts Treat Patients with Bullous Pemphigoid around the World? An International Survey. View Abstract
The effect of a third-dose BNT162b2 vaccine on anti-SARS-CoV-2 antibody levels in immunosuppressed patients. View Abstract
Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel. View Abstract
Short-Term Safety of Booster Immunization With BNT162b2 mRNA COVID-19 Vaccine in Healthcare Workers. View Abstract
Clinical efficacy of fecal microbial transplantation treatment in adults with moderate-to-severe atopic dermatitis. View Abstract
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry. View Abstract
The pathogenesis of melasma and implications for treatment. View Abstract
Association Between Vaccination With BNT162b2 and Incidence of Symptomatic and Asymptomatic SARS-CoV-2 Infections Among Health Care Workers. View Abstract
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population. View Abstract
The superiority of 72 h leukocyte descent over CRP for mortality prediction in patients with sepsis. View Abstract
Laboratory monitoring during antifungal treatment of paediatric tinea capitis. View Abstract
The Role of COVID-19 in Transitioning to a Better Pediatric Payment Model. View Abstract
A second C-reactive protein (CRP) test to detect inflammatory burst in patients with acute bacterial infections presenting with a first relatively low CRP. View Abstract
Multidisciplinary care of epidermolysis bullosa during the COVID-19 pandemic-Consensus: Recommendations by an international panel of experts. View Abstract
Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas. View Abstract
The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome. View Abstract
Griseofulvin vs terbinafine for paediatric tinea capitis: When and for how long. View Abstract
Telemedicine and Antibiotic Use: One Click Forward or Two Steps Back? View Abstract
Use of Social Psychology to Improve Adherence to National Bronchiolitis Guidelines. View Abstract
Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope. View Abstract
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis. View Abstract
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A. View Abstract
Ensuring Timely Connection to Early Intervention for Young Children With Developmental Delays. View Abstract
Fractional ablative carbon dioxide laser followed by topical sodium stibogluconate application: A treatment option for pediatric cutaneous leishmaniasis. View Abstract
Utilization of Patient Navigators in an Urban Academic Pediatric Primary Care Practice. View Abstract
Mechanisms Causing Loss of Keratinocyte Cohesion in Pemphigus. View Abstract
Epidermolytic Ichthyosis Sine Epidermolysis. View Abstract
Meeting Report of the Pathogenesis of Pemphigus and Pemphigoid Meeting in Munich, September 2016. View Abstract
SVEP1 plays a crucial role in epidermal differentiation. View Abstract
Assessment of the effectiveness of topical propranolol 4% gel for infantile hemangiomas. View Abstract
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome. View Abstract
Monopathogenic vs multipathogenic explanations of pemphigus pathophysiology. View Abstract
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis. View Abstract
Tinea capitis outbreak among paediatric refugee population, an evolving healthcare challenge. View Abstract
How Accountable Care Organizations Responded to Pediatric Incentives in the Alternative Quality Contract. View Abstract
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin. View Abstract
Analysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-?B. View Abstract
Definitions and outcome measures for mucous membrane pemphigoid: recommendations of an international panel of experts. View Abstract
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene. View Abstract
Report of the 10th Annual International Pachyonychia Congenita Consortium Meeting. View Abstract
Autosomal dominant inheritance of central centrifugal cicatricial alopecia in black South Africans. View Abstract
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting. View Abstract
Influence of glutathione S-transferase A1, P1, M1, T1 polymorphisms on oral busulfan pharmacokinetics in children with congenital hemoglobinopathies undergoing hematopoietic stem cell transplantation. View Abstract
Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutations. View Abstract
A systematic review of US state environmental legislation and regulation with regards to the prevention of neurodevelopmental disabilities and asthma. View Abstract
ABCA12 is the major harlequin ichthyosis gene. View Abstract
Partial treatment interruption of protease inhibitor-based highly active antiretroviral therapy regimens in HIV-infected children. View Abstract
The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: a comparative clinical, histologic, and immunohistochemical study. View Abstract
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