Marjorie McCracken, MD, PhD

Title(s)HS Clinical Professor, Pediatrics
SchoolSchool of Medicine
AddressLocation Required
Varies CA 00000
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    UC Berkeley, Berkeley,Ca.PhD12/1975Mathematics
    Stanford, Palo Alto, Ca.MD06/1985medicine
    Stanford, Palo Alto,Ca.pediatric residency07/1988Pediatrics
    UCSF, San Francisco,Ca.Pediatric GI Fellowship09/1990Pediatric Gastroenterology

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Solitary rectal ulcer syndrome in children and adolescents. J Pediatr Gastroenterol Nutr. 2012 Feb; 54(2):266-70. Perito ER, Mileti E, Dalal DH, Cho SJ, Ferrell LD, McCracken M, Heyman MB. PMID: 22094902; PMCID: PMC3719860.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    2. Sex differences in statural growth impairment in Crohn's disease: role of IGF-1. Inflamm Bowel Dis. 2011 Nov; 17(11):2318-25. Gupta N, Lustig RH, Kohn MA, McCracken M, Vittinghoff E. PMID: 21287667; PMCID: PMC3136638.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    3. Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins. J Pediatr. 2002 Nov; 141(5):695-700. Enns GM, Steiner RD, Buist N, Cowan C, Leppig KA, McCracken MF, Westphal V, Freeze HH, O'brien JF, Jaeken J, Matthijs G, Behera S, Hudgins L. PMID: 12410200.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
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