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Items: 1 to 20 of 76

1.

Teaching NeuroImages: Syntelencephaly: Middle interhemispheric fusion.

Arora A, Sahoo RK, Srivastava D.

Neurology. 2012 Sep 4;79(10):e86. doi: 10.1212/WNL.0b013e31826846f6. No abstract available.

PMID:
22946121
2.

[MR scanning of cerebrum in the investigation of delayed development in children. Syntelencephaly--is it really so rare?].

Schultz-Pedersen S, Balslev T, Christensen T.

Ugeskr Laeger. 2002 Sep 2;164(36):4188-90. Danish.

PMID:
12362834
3.

Syntelencephaly associated with connected transhemispheric cleft of focal cortical dysplasia.

Fujimoto S, Togari H, Banno T, Wada Y.

Pediatr Neurol. 1999 May;20(5):387-9.

PMID:
10371387
4.

Clinical features and outcomes of holoprosencephaly in Korea.

Ko JM, Kim SH.

Pediatr Neurol. 2010 Oct;43(4):245-52. doi: 10.1016/j.pediatrneurol.2010.05.001.

PMID:
20837302
5.

Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.

Lewis AJ, Simon EM, Barkovich AJ, Clegg NJ, Delgado MR, Levey E, Hahn JS.

Neurology. 2002 Dec 24;59(12):1860-5.

PMID:
12499474
6.

Middle interhemispheric variant of holoprosencephaly: a very mild clinical case.

Biancheri R, Rossi A, Tortori-Donati P, Stringara S, Bonifacino S, Minetti C.

Neurology. 2004 Dec 14;63(11):2194-6. No abstract available.

PMID:
15596788
7.

Middle interhemispheric variant of holoprosencephaly associated with bilateral perisylvian polymicrogyria.

Atalar MH, Icagasioglu D, Sener RN.

Pediatr Int. 2008 Apr;50(2):241-4. doi: 10.1111/j.1442-200X.2007.02311.x. No abstract available.

PMID:
18353069
8.

Unusual variant of holoprosencephaly in monosomy 13q.

Marcorelles P, Loget P, Fallet-Bianco C, Roume J, Encha-Razavi F, Delezoide AL.

Pediatr Dev Pathol. 2002 Mar-Apr;5(2):170-8.

PMID:
11910512
9.

Holoprosencephaly.

Hahn JS.

Handb Clin Neurol. 2008;87:13-37. doi: 10.1016/S0072-9752(07)87002-3. No abstract available.

PMID:
18809016
10.

Endocrine disorders associated with holoprosencephaly.

Hahn JS, Hahn SM, Kammann H, Barkovich AJ, Clegg NJ, Delgado MR, Levey E.

J Pediatr Endocrinol Metab. 2005 Oct;18(10):935-41.

PMID:
16355806
11.

Management of children with holoprosencephaly.

Levey EB, Stashinko E, Clegg NJ, Delgado MR.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):183-90. doi: 10.1002/ajmg.c.30254. Review.

PMID:
20104615
12.

Neuropathology of holoprosencephaly.

Marcorelles P, Laquerriere A.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):109-19. doi: 10.1002/ajmg.c.30249. Review.

PMID:
20104606
13.

Middle interhemispheric variant of holoprosencephaly: A rare midline malformation.

Rajalakshmi PP, Gadodia A, Priyatharshini P.

J Pediatr Neurosci. 2015 Jul-Sep;10(3):244-6. doi: 10.4103/1817-1745.165678.

14.

Coexistent holoprosencephaly and Chiari II malformation.

Rollins N, Joglar J, Perlman J.

AJNR Am J Neuroradiol. 1999 Oct;20(9):1678-81. Review.

15.

Clinical image. Middle interhemispheric variant of holoprosencephaly.

Posada M, Castillo M.

Pediatr Radiol. 2010 Nov;40(11):1843. doi: 10.1007/s00247-009-1479-z. Epub 2009 Dec 8. No abstract available.

PMID:
19997726
16.

Prenatal MR findings of the middle interhemispheric variant of holoprosencephaly.

Pulitzer SB, Simon EM, Crombleholme TM, Golden JA.

AJNR Am J Neuroradiol. 2004 Jun-Jul;25(6):1034-6.

17.

Holoprosencephaly survival and performance.

Barr M Jr, Cohen MM Jr.

Am J Med Genet. 1999 Jun 25;89(2):116-20. Review.

PMID:
10559767
18.

The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly.

Redlinger-Grosse K, Bernhardt BA, Berg K, Muenke M, Biesecker BB.

Am J Med Genet. 2002 Nov 1;112(4):369-78.

PMID:
12376939
19.

Syntelencephaly in an infant of a diabetic mother.

Robin NH, Ko LM, Heeger S, Muise KL, Judge N, Bangert BA.

Am J Med Genet. 1996 Dec 30;66(4):433-7.

PMID:
8989462
20.

Aventriculi associated with holoprosencephaly.

Kumar S, Jaiswal AK, Rastogi M.

J Clin Neurosci. 2006 Apr;13(3):378-80. Epub 2006 Mar 20.

PMID:
16546387

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