Fetal GM1-gangliosidosis: Morphological and biochemical studies-Reference-Cited by-同舟云学术

Fetal GM1-gangliosidosis: Morphological and biochemical studies

Published:1989-01 Issue:6 Volume:11 Page:394-398
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Ida Hiroyuki,Eto Yoshikatsu,Maekawa Kihei

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Chemical pathology of GM1-gangliosidosis (generalized gangliosidosis);Suzuki;J Neuropathol Exp Neurol,1969

2. The structure of oligosaccharides accumulating in the liver of GM1-gangliosidosis;Wolfe;J Biol Chem,1974

3. Presence of glycoprotein containing the polylactosamine structure in the brain and liver of GM1-gangliosidosis patients;Berra;Neurochem Pathol,1986

4. Late infantile systemic lipidosis: major monosialogangliosidosis: delineation of two types;Derry;Neurology,1968

5. Generalized gangliosidosis GM1 (Landing disease).Morphological disease;Roles;Eur Neurol,1970

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Infantile GM1-Gangliosidosis Revealed by Slate-Grey Mongolian Spots;The Open Pediatric Medicine Journal;2019-01-31

2. Development of lysosomal storage in mice with targeted disruption of the β-galactosidase gene: a model of human GM1-gangliosidosis;Brain and Development;2001-10

3. Síndrome de gangliosidosis infantil generalizada GMI. Presentación de dos casos;Revista de Neurología;1999

4. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991