144 related articles for article (PubMed ID: 7822735)
1. Atelencephalic aprosencephaly.
Harris CP; Townsend JJ; Norman MG; White VA; Viskochil DH; Pysher TJ; Klatt EC
J Child Neurol; 1994 Oct; 9(4):412-6. PubMed ID: 7822735
[TBL] [Abstract][Full Text] [Related]
2. Atelencephalic microcephaly: a case report and review of the literature.
Ippel PF; Breslau-Siderius EJ; Hack WW; van der Blij HF; Bouve S; Bijlsma JB
Eur J Pediatr; 1998 Jun; 157(6):493-7. PubMed ID: 9667407
[TBL] [Abstract][Full Text] [Related]
3. Atelencephalic microcephaly in a 21-week human fetus.
Siebert JR; Warkany J; Lemire RJ
Teratology; 1986 Aug; 34(1):9-19. PubMed ID: 3764783
[TBL] [Abstract][Full Text] [Related]
4. The vesicular forebrain (pseudo-aprosencephaly): a missing link in the teratogenetic spectrum of the defective brain anlage and its discrimination from aprosencephaly.
Sergi C; Schmitt HP
Acta Neuropathol; 2000 Mar; 99(3):277-84. PubMed ID: 10663970
[TBL] [Abstract][Full Text] [Related]
5. Atelencephalic microcephaly.
Garcia CA; Duncan C
Dev Med Child Neurol; 1977 Apr; 19(2):227-32. PubMed ID: 870360
[TBL] [Abstract][Full Text] [Related]
6. Aprosencephaly and cerebellar dysgenesis in sibs.
Florell SR; Townsend JJ; Klatt EC; Pysher TJ; Coffin CM; Wittwer CT; Viskochil DH
Am J Med Genet; 1996 Jun; 63(4):542-8. PubMed ID: 8826432
[TBL] [Abstract][Full Text] [Related]
7. [Neu-Laxova syndrome: Three case reports and a review of the literature].
Darouich S; Boujelbene N; Kehila M; Chanoufi MB; Reziga H; Gaigi S; Masmoudi A
Ann Pathol; 2016 Aug; 36(4):235-44. PubMed ID: 27475004
[TBL] [Abstract][Full Text] [Related]
8. [Holoprosencephaly: pathogenesis, phenotypic characteristics. About four cases].
Fatnassi R; Turki E; Belhaj J; Labidi I; Ben Regaya L; Hidar S; Khairi H
Morphologie; 2011 Sep; 95(310):79-82. PubMed ID: 21795094
[TBL] [Abstract][Full Text] [Related]
9. A fetus suggesting an extension of theXK-aprosencephaly spectrum phenotype.
Kajantie E; Ammälä P; Salonen R
Clin Dysmorphol; 2002 Oct; 11(4):299-301. PubMed ID: 12402000
[TBL] [Abstract][Full Text] [Related]
10. Which brain defects accompany cyclopia?
Lurie IW; Kirillova IA; Nedzved MK; Krapiva GA
Genet Couns; 1992; 3(3):127-32. PubMed ID: 1388930
[TBL] [Abstract][Full Text] [Related]
11. Prenatal evaluation of atelencephaly.
Nagaraj UD; Lawrence A; Vezina LG; Bulas DI; duPlessis AJ
Pediatr Radiol; 2016 Jan; 46(1):145-7. PubMed ID: 26260203
[TBL] [Abstract][Full Text] [Related]
12. Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
Lurie IW; Nedzved MK; Lazjuk GI; Kirillova IA; Cherstvoy ED
Am J Med Genet; 1979; 3(3):301-9. PubMed ID: 114053
[TBL] [Abstract][Full Text] [Related]
13. A review and case report of aprosencephaly and the XK aprosencephaly syndrome.
Martin RA; Carey JG
Am J Med Genet; 1982 Mar; 11(3):369-71. PubMed ID: 7081301
[No Abstract] [Full Text] [Related]
14. Aprosencephaly: histopathological features of the rudimentary forebrain and retina.
Kakita A; Hayashi S; Arakawa M; Takahashi H
Acta Neuropathol; 2001 Jul; 102(1):110-6. PubMed ID: 11547946
[TBL] [Abstract][Full Text] [Related]
15. Holoprosencephaly with agenesia of the prosencephalic ventricle.
Laure-Kamionowska M; Szymanska K; Klepacka T
Folia Neuropathol; 2015; 53(4):387-94. PubMed ID: 26785373
[TBL] [Abstract][Full Text] [Related]
16. Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?
McPherson E; Huff D; Dunn J; Muenke M
Birth Defects Res A Clin Mol Teratol; 2004 Aug; 70(8):537-44. PubMed ID: 15329833
[TBL] [Abstract][Full Text] [Related]
17. Anomalies of cerebral structures in acranial neonates.
Dambska M; Schmidt-Sidor B; Maslinska D; Laure-Kamionowska M; Kosno-Kruszewska E; Deregowski K
Clin Neuropathol; 2003; 22(6):291-5. PubMed ID: 14672507
[TBL] [Abstract][Full Text] [Related]
18. Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Winter TC; Kennedy AM; Woodward PJ
Radiographics; 2015; 35(1):275-90. PubMed ID: 25590404
[TBL] [Abstract][Full Text] [Related]
19. Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst.
Kim TS; Cho S; Dickson DW
Acta Neuropathol; 1990; 79(4):424-31. PubMed ID: 2339594
[TBL] [Abstract][Full Text] [Related]
20. Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significance.
den Hollander NS; Wessels MW; Los FJ; Ursem NT; Niermeijer MF; Wladimiroff JW
Ultrasound Obstet Gynecol; 2000 Apr; 15(4):282-7. PubMed ID: 10895445
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
