Literature DB >> 3818002

Genetic aspects of congenital cerebellar ataxia.

D Kumar.   

Abstract

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Year:  1986        PMID: 3818002     DOI: 10.1007/bf02748571

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


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  33 in total

1.  The Dandy-Walker syndrome. A clinicopathological study based on 28 cases.

Authors:  M N Hart; N Malamud; W G Ellis
Journal:  Neurology       Date:  1972-08       Impact factor: 9.910

2.  The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment.

Authors:  B Hagberg; G Sanner; M Steen
Journal:  Acta Paediatr Scand Suppl       Date:  1972

3.  Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome).

Authors:  K H Gustavson; A Kreuger; P O Petersson
Journal:  Clin Genet       Date:  1971       Impact factor: 4.438

4.  Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks.

Authors:  J C Murray; J A Johnson; T D Bird
Journal:  Clin Genet       Date:  1985-10       Impact factor: 4.438

5.  CNS anomalies and the midline as a "developmental field".

Authors:  J M Opitz; E F Gilbert
Journal:  Am J Med Genet       Date:  1982-08

6.  Joubert-Boltshauser syndrome with polydactyly in siblings.

Authors:  J Egger; M H Bellman; E M Ross; M Baraitser
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-08       Impact factor: 10.154

7.  Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis.

Authors:  E Boltshauser; W Isler
Journal:  Neuropadiatrie       Date:  1977-02

8.  Encephalocele (cerebellocele) in the Goldenhar-Gorlin syndrome.

Authors:  S Aleksic; G Budzilovich; M A Greco; F Epstein; I Feigin; J Pearson
Journal:  Eur J Pediatr       Date:  1983-04       Impact factor: 3.183

9.  [Joubert's syndrome. Apropos of 5 cases].

Authors:  J Aicardi; M E Castello-Branco; C Roy
Journal:  Arch Fr Pediatr       Date:  1983-10

10.  A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment.

Authors:  J C Christian; R N Dexter; C G Palmer; J Muller
Journal:  Am J Med Genet       Date:  1980
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