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infantile persistent hypoglycemia caused by hypermsulinemia相关文献:
Shashi-Pena Syndrome.
Porter JM, Pena LDM, Spillmann RC, Johnson A, Shashi V.
2024 Nov 7. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:39527683
Nesidioblastosis in adults.
Dravecka I, Lazurova I.
Neoplasma. 2014;61(3):252-6. doi: 10.4149/neo_2014_047.
PMID:24645840
Brain glucose supply and the syndrome of infantile neuroglycopenia.
Pascual JM, Wang D, Hinton V, Engelstad K, Saxena CM, Van Heertum RL, De Vivo DC.
Arch Neurol. 2007 Apr;64(4):507-13. doi: 10.1001/archneur.64.4.noc60165. Epub 2007 Feb 12.
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A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.
Yasuda K, Koda N, Kadowaki H, Ogawa Y, Kimura S, Kadowaki T, Akanuma Y.
Intern Med. 2001 Jan;40(1):32-7. doi: 10.2169/internalmedicine.40.32.
PMID:11201367
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