Literature DB >> 13354244

Oligophrenia combined with congenital ichthyosiform erythrodermia, spastic syndrome and macularretinal degeneration; a clinical and genetic study.

T SJOGREN.   

Abstract

Entities:  

Keywords:  HEREDITY; ICHTHYOSIS; MENTAL DEFICIENCY/complications

Mesh：

Year:  1956        PMID： 13354244

Source DB:  PubMed          Journal:  Acta Genet Stat Med        ISSN： 0567-7440


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  8 in total

1.  Congenital ichthyosis, mental retardation and spasticity (Sjogren-Larsson syndrome).

Authors:  W A ZALESKI
Journal:  Can Med Assoc J       Date:  1962-05-19       Impact factor: 8.262

Review 2.  [Skin and teeth].

Authors:  J Heinlin; N Heinlin; J Steinbauer; M Landthaler; S Karrer
Journal:  Hautarzt       Date:  2009-07       Impact factor: 0.751

3.  Computed tomography in Sjögren-Larsson syndrome.

Authors:  J M Gomori; V Leibovici; A Zlotogorski; I Wirguin; S Haham-Zadeh
Journal:  Neuroradiology       Date:  1987       Impact factor: 2.804

4.  Sjögren-Larsson syndrome in two sibs with peripheral nerve involvement and bisalbuminaemia.

Authors:  M Maia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-12       Impact factor: 10.154

5.  Sjögren-Larsson syndrome in a Turkish family.

Authors:  B S Sayli; I Erüreten; U Topuz
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

Review 6.  Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.

Authors:  William B Rizzo
Journal:  Mol Genet Metab       Date:  2006-09-22       Impact factor: 4.797

Review 7.  Sjögren-Larsson syndrome. Oligophrenia--ichthyosis--di-tetraplegia.

Authors:  U Theile
Journal:  Humangenetik       Date:  1974-05-17

Review 8.  Sjogren-Larsson Syndrome: Mechanisms and Management.

Authors:  Parayil Sankaran Bindu
Journal:  Appl Clin Genet       Date:  2020-01-07
  8 in total

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