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congenital enteric atresia 相关文献:
The developmental etiology and pathogenesis of Hirschsprung disease.
Butler Tjaden NE, Trainor PA.
Transl Res. 2013 Jul;162(1):1-15. doi: 10.1016/j.trsl.2013.03.001. Epub 2013 Mar 22.
PMID:23528997
A case of split notochord syndrome with congenital ileal atresia, the total absence of a colon, and a dorsal enteric cyst communicating to the retroperitoneal isolated ceca with a vesical fistula.
Asagiri K, Yagi M, Tanaka Y, Akaiwa M, Asakawa T, Kaida A, Kobayashi H, Tanaka H.
Pediatr Surg Int. 2008 Sep;24(9):1073-7. doi: 10.1007/s00383-008-2206-9. Epub 2008 Jul 30.
PMID:18665369
Regenerative medicine: postnatal approaches.
Tam PKH, Wong KKY, Atala A, Giobbe GG, Booth C, Gruber PJ, Monone M, Rafii S, Rando TA, Vacanti J, Comer CD, Elvassore N, Grikscheit T, de Coppi P.
Lancet Child Adolesc Health. 2022 Sep;6(9):654-666. doi: 10.1016/S2352-4642(22)00193-6.
PMID:35963270
Trichohepatoenteric Syndrome.
Fabre A, Bourgeois P, Chaix C, Bertaux K, Goulet O, Badens C.
2018 Jan 11. 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:29334452
Hirschprung's disease.
Sullivan PB.
Arch Dis Child. 1996 Jan;74(1):5-7. doi: 10.1136/adc.74.1.5.
PMID:8660047
Causes and consequences: development and pathophysiology of Hirschsprung disease.
Burns AJ, Goldstein AM.
World J Pediatr Surg. 2024 Nov 25;7(4):e000903. doi: 10.1136/wjps-2024-000903. eCollection 2024.
PMID:39600627
Congenital agastria.
Dorney SF, Middleton AW, Kozlowski K, Benjamin BN, Kan AE, Kamath KR.
J Pediatr Gastroenterol Nutr. 1987 Mar-Apr;6(2):307-10. doi: 10.1097/00005176-198703000-00026.
PMID:3694355
Treatment and Prevention of Neurocristopathies.
Pilon N.
Trends Mol Med. 2021 May;27(5):451-468. doi: 10.1016/j.molmed.2021.01.009. Epub 2021 Feb 22.
PMID:33627291
Enteric duplication in children.
Sujka JA, Sobrino J, Benedict LA, Alemayehu H, Peter SS, Hendrickson R.
Pediatr Surg Int. 2018 Dec;34(12):1329-1332. doi: 10.1007/s00383-018-4362-x. Epub 2018 Oct 13.
PMID:30315502
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M.
J Clin Invest. 2022 May 16;132(10):e154997. doi: 10.1172/JCI154997.
PMID:35575086
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