Detalhe da pesquisa
1.
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation.
Neuropathol Appl Neurobiol
; 43(7): 631-635, 2017 12.
Artigo
Inglês
| MEDLINE | ID: mdl-28489313
2.
Overexpression of GRP78 in complete hydatidiform moles.
Gynecol Oncol
; 125(3): 580-4, 2012 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22425662
3.
Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.
Kidney Int
; 77(4): 350-8, 2010 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-19940839
4.
[Expression of the elastic fibers components during the fÅtal liver development]. / Expression des composants de la matrice élastique au cours du développement hépatique fÅtal.
Morphologie
; 94(307): 87-92, 2010 Nov.
Artigo
Francês
| MEDLINE | ID: mdl-20920872
5.
Molecular heterogeneity in fetal forms of type II lissencephaly.
Hum Mutat
; 28(10): 1020-7, 2007 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-17559086
6.
[Perinatal prognosis of pregnancies complicated by placental chronic intervillitis]. / Pronostic périnatal des grossesses compliquées d'intervillites chroniques placentaires.
J Gynecol Obstet Biol Reprod (Paris)
; 35(7): 711-9, 2006 Nov.
Artigo
Francês
| MEDLINE | ID: mdl-17088773
7.
[DiGeorge syndrome, a review of 52 patients]. / Syndrome de Di George, étude rétrospective de 52 cas.
Arch Pediatr
; 12(3): 254-7, 2005 Mar.
Artigo
Francês
| MEDLINE | ID: mdl-15734119
8.
Molecular anatomy of the development of the human substantia nigra.
J Comp Neurol
; 379(1): 72-87, 1997 Mar 03.
Artigo
Inglês
| MEDLINE | ID: mdl-9057113
9.
Ontogeny of the striatal neurons expressing neuropeptide genes in the human fetus and neonate.
J Comp Neurol
; 360(3): 488-505, 1995 Sep 25.
Artigo
Inglês
| MEDLINE | ID: mdl-8543654
10.
Ontogeny of the striatal neurons expressing the D1 dopamine receptor in humans.
J Comp Neurol
; 370(1): 23-34, 1996 Jun 17.
Artigo
Inglês
| MEDLINE | ID: mdl-8797154
11.
Expression of NGF receptors in normal and pathological human thymus.
J Neuroimmunol
; 85(1): 11-21, 1998 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-9626993
12.
Differential expression of the nm23 genes in the developing human trophoblast.
Placenta
; 25(1): 20-8, 2004 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-15013635
13.
Splenogonadal fusion limb defect syndrome: report of five new cases and review.
Am J Med Genet
; 86(4): 347-58, 1999 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-10494091
14.
Ventricular patch endocarditis caused by Propionibacterium acnes: advantages of gallium scanning.
J Infect
; 43(4): 249-51, 2001 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-11869063
15.
Idiopathic arterial calcification in a stillborn complicated by pleural hemorrhage and hydrops fetalis.
Arch Pathol Lab Med
; 116(3): 293-5, 1992 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-1536617
16.
Laryngomucocele as an unusual late complication of subtotal laryngectomy. Case report.
Ann Otol Rhinol Laryngol
; 107(8): 703-7, 1998 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-9716874
17.
Trisomy 22 with thyroid isthmus agenesis and absent gall bladder.
Genet Couns
; 15(3): 311-5, 2004.
Artigo
Inglês
| MEDLINE | ID: mdl-15517823
18.
Horizontal glottectomy: functional and oncological results.
J Laryngol Otol
; 111(9): 833-8, 1997 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-9373549
19.
[Anatomo-pathological diagnosis of neonatal malformations of the urinary tract. II. Excreto-urinary tract malformations]. / Diagnostic anatomo-pathologique des malformations néo-natales de l'appareil urinaire. II. Malformations des voies excréto-urinaires.
Ann Pathol
; 4(2): 157-61, 1984.
Artigo
Francês
| MEDLINE | ID: mdl-6732908
20.
[Anatomo-pathologic diagnosis of neonatal malformations of the urinary tract. 1: Malformations of the kidney parenchyma]. / Diagnostic anatomo-pathologique des malformations néo-natales de l'appareil urinaire. 1re partie: Malformations du parenchyme rénal.
Ann Pathol
; 4(1): 69-77, 1984.
Artigo
Francês
| MEDLINE | ID: mdl-6704210