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Literature DB >> 13030653

A type of congenital ocular motor apraxia presenting jerky head movements.

D G COGAN.

Abstract

Entities: Disease

Keywords: APRAXIA; MUSCLES, OCULOMOTOR/abnormalities

Mesh：

Year: 1953 PMID： 13030653 DOI： 10.1016/0002-9394(53)90553-4

Source DB: PubMed Journal: Am J Ophthalmol ISSN： 0002-9394 Impact factor: 5.258

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Cited

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11 in total

1. Clinical and electro-oculographically obtained viewpoints for the evaluation of conjugate paralysis and nystagmus

Authors: H F PIPER; G HOLLAND
Journal: Albrecht Von Graefes Arch Ophthalmol Date: 1960

2. Saccade initiation in ocular motor apraxia.

Authors: H Rambold; A Moser; B Zurowski; J Gbadamosi; D Kömpf; A Sprenger; C Helmchen
Journal: J Neurol Date: 2006-04-20 Impact factor: 4.849

3. MRI with fibre tracking in Cogan congenital oculomotor apraxia.

Authors: Laura Merlini; Maria I Vargas; Raoul De Haller; Bénédict Rilliet; Joel Fluss
Journal: Pediatr Radiol Date: 2010-05-07

Review 4. New autosomal recessive cerebellar ataxias with oculomotor apraxia.

Authors: Isabelle Le Ber; Alexis Brice; Alexandra Dürr
Journal: Curr Neurol Neurosci Rep Date: 2005-09 Impact factor: 5.081

5. 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

6. Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.

Authors: Barbara Castellotti; Caterina Mariotti; Marco Rimoldi; Roberto Fancellu; Massimo Plumari; Sara Caimi; Graziella Uziel; Nardo Nardocci; Isabella Moroni; Giovanna Zorzi; Davide Pareyson; Daniela Di Bella; Stefano Di Donato; Franco Taroni; Cinzia Gellera
Journal: Neurogenetics Date: 2011-04-05 Impact factor: 2.660

A type of congenital ocular motor apraxia presenting jerky head movements.

1. Clinical and electro-oculographically obtained viewpoints for the evaluation of conjugate paralysis and nystagmus

2. Saccade initiation in ocular motor apraxia.

3. MRI with fibre tracking in Cogan congenital oculomotor apraxia.

Review 4. New autosomal recessive cerebellar ataxias with oculomotor apraxia.

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

6. Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.

Review 7. An overview of the patient with ataxia.

8. Ocular motor apraxia after sequential bilateral striatal infarctions.

9. Saccades and eye-head coordination in ataxia with oculomotor apraxia type 2.

10. Electroretinographic findings in congenital oculomotor apraxia (Cogan's syndrome).