Literature DB >> 4194292

The accumulation of cerebroside sulfates by fibroblasts in culture from patients with late infantile metachromatic leukocystrophy.

M T Porter, A L Fluharty, S E Harris, H Kihara.   

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Year:  1970        PMID： 4194292     DOI： 10.1016/0003-9861(70)90392-9

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN： 0003-9861            Impact factor:   4.013


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  13 in total

Review 1.  Investigation of degenerative disease of the central nervous system.

Authors:  J Wilson
Journal:  Arch Dis Child       Date:  1972-04       Impact factor: 3.791

2.  Simplified procedure for preparation of 35S-labeled brain sulfatide.

Authors:  A L Fluharty; M L Davis; H Kihara; G Kritchevsky
Journal:  Lipids       Date:  1974-11       Impact factor: 1.880

Review 3.  Genetic heterogeneity in metachromatic leukodystrophy.

Authors:  H Kihara
Journal:  Am J Hum Genet       Date:  1982-03       Impact factor: 11.025

4.  High-resolution loading tests in the study of genetic heterogeneity in gangliosidosis fibroblasts.

Authors:  V S Akhunov; T V Mirenburg; X D Krasnopolskaya
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

5.  Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders.

Authors:  B Schmid; B C Paton; K Sandhoff; K Harzer
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

6.  The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsy.

Authors:  A F Hahn; B A Gordon; J J Gilbert; G G Hinton
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

7.  Late infantile metachromatic leucodystrophy (MLD). Clinical and diagnostic evaluation in a typical case.

Authors:  L N Rossi; F Vassella; A Bischoff; U N Wiesmann; N Herschkowitz
Journal:  J Neurol       Date:  1975-10-24       Impact factor: 4.849

8.  Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.

Authors:  Y Eto; S Numaguchi; T Tahara; O M Rennert
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183

9.  Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.

Authors:  T Tønnesen; C Vrang; U N Wiesmann; H Christomanou; H O Lou
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Diagnosis of metachromatic leukodystrophy, Krabbe disease, and Farber disease after uptake of fatty acid-labeled cerebroside sulfate into cultured skin fibroblasts.

Authors:  T Kudoh; D A Wenger
Journal:  J Clin Invest       Date:  1982-07       Impact factor: 14.808
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