Literature DB >> 4239322

Clinical, biochemical and ultrastructural studies of an atypical form of mucopolysaccharidosis.

H Loeb, M Tondeur, M Toppet, N Cremer.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1969        PMID: 4239322     DOI: 10.1111/j.1651-2227.1969.tb04710.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


× No keyword cloud information.
  7 in total

1.  Mannosidosis: tissue culture studies in relation to prenatal diagnosis.

Authors:  I Maire; M T Zabot; M Mathieu; J Cotte; M Hermier
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies.

Authors:  M Haltia; J Palo; S Autio
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

3.  The genetic mucolipidoses. Diagnosis and differential diagnosis.

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

4.  Lysosomes and mucopolysaccharidoses.

Authors:  H G Hers; F van Hoof
Journal:  Biochem J       Date:  1969-12       Impact factor: 3.857

5.  The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.

Authors:  G Bach; R Friedman; B Weissmann; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1972-08       Impact factor: 11.205

6.  Spectrum of mutations in alpha-mannosidosis.

Authors:  T Berg; H M Riise; G M Hansen; D Malm; L Tranebjaerg; O K Tollersrud; O Nilssen
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

7.  Lipid composition of whole brain and cerebellum in Hurler syndrome (MPS IH) mice.

Authors:  Karie A Heinecke; Brandon N Peacock; Bruce R Blazar; Jakub Tolar; Thomas N Seyfried
Journal:  Neurochem Res       Date:  2011-01-21       Impact factor: 4.414

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.