Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

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Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

@yue

2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

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Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

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Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

@en

P1476

Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

@en

P2093

Aidin Tabrizi

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Mohammad Barzegar

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Mohammad Sayadnasiri

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P2860

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia

Neurological manifestations of the oculodentodigital dysplasia syndrome

Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene

Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter

Oculodentodigital dysplasia. Four new reports and a literature review.

Oculodental digital dysplasia: neuroimaging in a kindred.

Oculodentodigital dysplasia: ulnar-sided syndactyly and its associated disorders.

Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.

Ataxia, chorea, seizures, and dementia. Pathologic features of a newly defined familial disorder.

Oculodentodigital dysplasia: disease spectrum in an eight-year-old boy, his parents and a sibling

P304

39-43

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P31

scholarly article

case report

P433

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P478

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P577

2012-01-01T00:00:00Z

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P698

24665271

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P932

3943032

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