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Abdollah Sadeghi-Nejad, MD, Pediatric Endocrinology, Boston, MA, MetroWest Medical Center

AbdollahSadeghi-NejadMD

Pediatric Endocrinology Boston, MA

Professor, Pediatrics, Tufts Medical Center

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Education & Training

  • University of California (San Francisco)
    University of California (San Francisco)Fellowship, Pediatric Endocrinology, 1969 - 1970
  • Tufts Medical Center
    Tufts Medical CenterResidency, Pediatrics, 1967 - 1969
  • University of Chicago
    University of ChicagoResidency, Pediatrics, 1965 - 1967
  • University of Chicago
    University of ChicagoInternship, Transitional Year, 1964 - 1965
  • University of Chicago Division of the Biological Sciences The Pritzker School of Medicine
    University of Chicago Division of the Biological Sciences The Pritzker School of MedicineClass of 1964
  • University of Chicago
    University of ChicagoM.S., 1964
  • University of Chicago
    University of ChicagoM.S., Pathology, 1964
  • Beloit College
    Beloit CollegeB.S., Cum Laude, 1960

Certifications & Licensure

  • CA State Medical License
    CA State Medical License 1969 - Present
  • MA State Medical License
    MA State Medical License 1970 - 2025
  • American Board of Pediatrics Pediatrics
  • American Board of Pediatrics Pediatric Endocrinology

Awards, Honors, & Recognition

  • Distinguished Faculty Tufts University School of Medicine, 2003
  • Boston Magazine Castle Connolly, 2011-2014
  • Best Doctors in America Best Doctors in America, 1994-2014
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Publications & Presentations

PubMed

Journal Articles

  • Role of RET protein-tyrosine kinase inhibitors in the treatment of RET-driven thyroid and lung cancers  
    Roskoski R Jr, Sadeghi-Nejad A, Pharmacol Res, 1/1/2018
  • Gender reversal and bilateral giant adrenal myelolipomas in a 46-XX patient with 21-hydroxylase deficiency: case report and review of the literature  
    Westcott GP, Sadeghi-Nejad A, Munoz-Pena J, Blau A, Goodman M, Siegel RD, AACE Clinical Care Rep, 1/1/2017
  • HESX1 Mutations in Patients with Congenital Hypopituitarism: Variable Phenotypes with the Same Genotype  
    Fang Q, Flavia A, Benedetti F, Ma Q, Gregory L, Li JZ, Dattani M SadeghiNejad A, Arnhold IJP, Bilharinho de Mendon�a B, Camper SA, Carvalho LR, Clinical Endocr, 1/1/2016
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Books/Book Chapters

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Abstracts/Posters

  • HESX1 Mutations Can be Present as a Spectrum Disorder from Craniofacial Defects to Hypopituitarism
    Benedetti AF Fang Q, Ma Q, Li JZ, Dattani MT, Gregory LC, Sadeghi-Nejad A, Arnhold IJP, Bilharinho Mendonca B, Camper SA, Carvalho LRS, Endocrine Society, 1/1/2016
  • Phenotypic Spectrum from Cerebral Midline Defects to Hypopituitarism: Examples from HESX1 mutations
    Fang Q, Ma Q, Sadeghi-Nejad A, Arnhold IJP, Correa FA, Ozel AB, Li JZ, Camper SA, Carvalho LRS, American Society of Human Genetics, 1/1/2015
  • Spontaneous somatic mutation resulting in PHEX mosaicism in a boy with familial hypophosphatemic rickets
    Bansal S, Sadeghi-Nejad A., Pediatric Academic Societies, 1/1/2012
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Other

  • Hyperinsulinism 
    Sinha S, Chan KK, Sadeghi-Nejad A, Pediatrics, e-Medicine
    http://emedicine.medscape.com/article/921258
    1/1/2014
  • Hyperinsulinemia 
    Chan K.C., Sadeghi-Nejad, A., Pediatrics, e-Medicine
    1/1/2001
  • Hyperthyroidism 
    Gold J.G., Sadeghi-Nejad, A., Pediatrics, e-Medicine
    1/1/2001

Professional Memberships

Hospital Affiliations