Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report-Reference-Cited by-同舟云学术

Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report

Published:2017-05-19 Issue:1 Volume:18 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Hilbrands Robert,Keymolen Kathelijn,Michotte Alex,Marichal Miriam,Cools Filip,Goossens Anieta,Veld Peter In’t,De Schepper Jean,Hattersley Andrew,Heimberg Harry^ORCID

Funder

VUB Research Council

Universitaire stichting België

Fund for Scientific Research Flanders (FWO)

Wellcome Trust Senior Investigator

NIHR Senior Investigator

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-017-0419-2.pdf

Reference24 articles.

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2. Pearson ER, Flechtner I, Njolstad PR, Malecki MT, Flanagan SE, Larkin B, Ashcroft FM, Klimes I, Codner E, Iotova V, et al. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med. 2006;355(5):467–77.

3. Murphy R, Ellard S, Hattersley AT. Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes. Nat Clin Pract Endocrinol Metab. 2008;4(4):200–13.

4. Flechtner I, Vaxillaire M, Cave H, Scharfmann R, Froguel P, Polak M. Neonatal hyperglycaemia and abnormal development of the pancreas. Best Pract Res Clin Endocrinol Metab. 2008;22(1):17–40.

5. Schwitzgebel VM. Many faces of monogenic diabetes. J Diab Invest. 2014;5(2):121–33.

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