Literature DB >> 5001028

Clinical and neuropathological investigations of four cases of holoprosencephaly with arhinencephaly.

M Habedank, E Thomas.   

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Year:  1970        PMID： 5001028     DOI： 10.1055/s-0028-1091850

Source DB:  PubMed          Journal:  Neuropadiatrie        ISSN： 0028-3797


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  6 in total

1.  Partial trisomy 13q21toqter de novo due to a recombinant chromosome rec(13)dup q.

Authors:  M Habedank
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

2.  Cranial morphology in the 18p-syndrome.

Authors:  J Faust; F Kotlarek; M Habedank
Journal:  Eur J Pediatr       Date:  1978-08-17       Impact factor: 3.183

3.  The 18 p-syndrome. Report of four cases.

Authors:  J Faust; M Habedank; C Nieuwenhuijsen
Journal:  Eur J Pediatr       Date:  1976-08-16       Impact factor: 3.183

4.  Holoprosencephaly and related entities.

Authors:  C R Fitz
Journal:  Neuroradiology       Date:  1983       Impact factor: 2.804

5.  Histopathological study of alobar holoprosencephaly. 2. Marginal glioneural heterotopia and other gliomesenchymal abnormalities.

Authors:  M Mizuguchi; Y Morimatsu
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

6.  Trilobar holoprosencephaly ("triprosencephaly"): a unique type of cerebral malformation.

Authors:  P R Mazal; G Schuhfried; H Budka
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088
  6 in total

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