Literature DB >> 4216890

I-cell disease--mucolipidosis II.

N Gordon.   

Abstract

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Mesh：

Year:  1973        PMID： 4216890      PMCID： PMC2495859          DOI： 10.1136/pgmj.49.571.359

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN： 0032-5473            Impact factor:   2.401


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  4 in total

1.  I-cell disease: a clinical picture.

Authors:  J G Leroy; J W Spranger; M Feingold; J M Opitz; A C Crocker
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

2.  Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture.

Authors:  M Tondeur; E Vamos-Hurwitz; S Mockel-Pohl; J P Dereume; N Cremer; H Loeb
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

3.  The genetic mucolipidoses. Diagnosis and differential diagnosis.

Authors:  J W Spranger; H R Wiedemann
Journal:  Humangenetik       Date:  1970

4.  Lipid abnormalities in a variant of the Hurler syndrome.

Authors:  R Matalon; J A Cifonelli; H Zellweger; A Dormanfman
Journal:  Proc Natl Acad Sci U S A       Date:  1968-04       Impact factor: 11.205
  4 in total
  2 in total

1.  I-cell disease (Mucolipidosis II).

Authors:  M Kabra; S Gulati; M Kaur; J Sharma; A Singh; V Chopra; P S Menon; V Kalra
Journal:  Indian J Pediatr       Date:  2000-09       Impact factor: 1.967

2.  Hip Morphology in Mucolipidosis Type II.

Authors:  Luise Sophie Ammer; Esmeralda Oussoren; Nicole Maria Muschol; Sandra Pohl; Maria Estela Rubio-Gozalbo; René Santer; Ralf Stuecker; Eik Vettorazzi; Sandra Rafaela Breyer
Journal:  J Clin Med       Date:  2020-03-08       Impact factor: 4.241
  2 in total

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