Literature DB >> 4643438

Cogan's congenital ocular motor apraxia in two successive generations.

F Vassella, J Lütschg, M Mumenthaler.   

Abstract

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Year:  1972        PMID： 4643438     DOI： 10.1111/j.1469-8749.1972.tb03322.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


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  6 in total

1.  Computed tomography in congenital ocular motor apraxia.

Authors:  I Eda; S Takashima; T Kitahara; K Ohno; K Takeshita
Journal:  Neuroradiology       Date:  1984       Impact factor: 2.804

2.  Congenital horizontal gaze palsy and kyphoscoliosis in two brothers.

Authors:  E Riley; M Swift
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

3.  Pseudodominant inheritance of nephronophthisis caused by a homozygous NPHP1 deletion.

Authors:  Julia Hoefele; Ahmet Nayir; Moumita Chaki; Anita Imm; Susan J Allen; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Pediatr Nephrol       Date:  2011-01-22       Impact factor: 3.714

4.  Intermittent horizontal saccade failure ('ocular motor apraxia') in children.

Authors:  C M Harris; F Shawkat; I Russell-Eggitt; J Wilson; D Taylor
Journal:  Br J Ophthalmol       Date:  1996-02       Impact factor: 4.638

5.  The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.

Authors:  Melissa A Parisi; Craig L Bennett; Melissa L Eckert; William B Dobyns; Joseph G Gleeson; Dennis W W Shaw; Ruth McDonald; Allison Eddy; Phillip F Chance; Ian A Glass
Journal:  Am J Hum Genet       Date:  2004-05-11       Impact factor: 11.025

6.  Torticollis, head bobbing and oscillatory eye movements in a 14 year old child.

Authors:  Kalyan B Bhattacharyya; B K Roy; A K Dutta; B Mondal; P Biswas
Journal:  Ann Indian Acad Neurol       Date:  2016 Jan-Mar       Impact factor: 1.383
  6 in total

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