(Q34018171)

30 July 2017

title

Ophthalmologic findings in Cohen syndrome. A long-term follow-up (English)

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30 July 2017

Kivitie-Kallio S

1

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30 July 2017

Summanen P

series ordinal

2

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30 July 2017

Raitta C

series ordinal

3

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30 July 2017

Norio R

series ordinal

4

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30 July 2017

publication date

1 September 2000

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30 July 2017

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30 July 2017

volume

107

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30 July 2017

issue

9

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30 July 2017

page(s)

1737-1745

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A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Neurological and psychological findings in patients with Cohen syndrome: a study of 18 patients aged 11 months to 57 years

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

MRI of the brain in the Cohen syndrome: a relatively large corpus callosum in patients with mental retardation and microcephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Granulocytopenia in Cohen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Periodontal findings in Cohen syndrome with chronic neutropenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome: evaluation of its cardiac, endocrine and radiological features

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Confirmation of the Cohen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

The Cohen syndrome: clinical and endocrinological studies of two new cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cardiac involvement in the Cohen syndrome: a case report.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome: further delineation and inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

The clinical features of the Cohen syndrome: further case reports

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome with bull's eye macular lesion.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

[Cohen syndrome in 2 brothers]

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome: a connective tissue disorder?

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type?

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

The Cohen syndrome. Retinal lesions and granulocytopenia

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Growth hormone deficiency in a girl with the Cohen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Multiple coagulation defects and the Cohen syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Identical twins with Cohen syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Cohen syndrome: the clinical symptoms and stigmata at a young age.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Lens opacity meter: a new instrument to quantify lens opacity

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Lens opacity: a population study

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Changes in the electroretinogram and visual evoked potentials during general anaesthesia using enflurane.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Incidence of myopia in a population of Finnish school children

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Are the Mirhosseini-Holmes-Walton syndrome and the Cohen syndrome identical?

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

Investigations into the Aqueous Humour Dynamics in Primary Pigmentary Degeneration of the Retina

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2800%2900279-7

7 January 2021

10.1016/S0161-6420(00)00279-7

Identifiers

DOI

1 reference

30 July 2017

1 reference