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1.
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
Hum Mol Genet
; 32(13): 2192-2204, 2023 06 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-37010102
2.
A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus.
Neuropediatrics
; 49(3): 222-224, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29642246
3.
Gastric ulceration and perforation secondary to large trichobezoar - A case report describing the role of magnetic resonance imaging in diagnosis.
Int J Surg Case Rep
; 43: 25-28, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29438853
4.
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.
Ital J Pediatr
; 44(1): 34, 2018 Mar 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29523172
5.
[Sepsis--current aspects].
Khirurgiia (Sofiia)
; (2-3): 28-33, 2010.
Artículo
en Búlgaro
| MEDLINE | ID: mdl-21972692
6.
[Improved technique for internal biliary-digestive drainage during conventional palliative procedure of nonresectable tumors of periampullary region].
Khirurgiia (Sofiia)
; (1-2): 20-3, 2008.
Artículo
en Búlgaro
| MEDLINE | ID: mdl-18983004
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