Literature DB >> 4119025

Metachromatic leucodystrophy. Two unusual cases of the late infantile form.

R Nyberg-Hansen.   

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Year:  1972        PMID: 4119025

Source DB:  PubMed          Journal:  Z Neurol        ISSN: 0012-1037


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  12 in total

1.  A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM.

Authors:  J H AUSTIN; A S BALASUBRAMANIAN; T N PATTABIRAMAN; S SARASWATHI; D K BASU; B K BACHHAWAT
Journal:  J Neurochem       Date:  1963-12       Impact factor: 5.372

2.  EVIDENCE FOR THE GENETIC BLOCK IN METACHROMATIC LEUCODYSTROPHY (ML).

Authors:  E MEHL; H JATZKEWITZ
Journal:  Biochem Biophys Res Commun       Date:  1965-05-03       Impact factor: 3.575

3.  [On metachromatic leukodystrophy (Scholz type)].

Authors:  J PEIFFER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1959

4.  Screening for metabolic disorders using gas-liquid chromatography, mass spectrometry, and computer technique.

Authors:  E Jellum; O Stokke; L Eldjarn
Journal:  Scand J Clin Lab Invest       Date:  1971-05       Impact factor: 1.713

5.  Cerebroside 3-sulfate as a physiological substrate of arylsulfatase A.

Authors:  E Mehl; H Jatzkewitz
Journal:  Biochim Biophys Acta       Date:  1968-03-25

6.  Metachromatic leucodystrophy in early childhood. Treatment with a diet deficient in vitamin A.

Authors:  J C Melchior; J Clausen
Journal:  Acta Paediatr Scand       Date:  1968-01

7.  A versatile lithium buffer elution system for single column automatic amino acid chromatography.

Authors:  T L Perry; D Stedman; S Hansen
Journal:  J Chromatogr       Date:  1968-12-17

8.  Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML).

Authors:  H Jatzkewitz; E Mehl
Journal:  J Neurochem       Date:  1969-01       Impact factor: 5.372

9.  Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis.

Authors:  J Austin; D Armstrong; S Fouch; C Mitchell; D Stumpf; L Shearer; O Briner
Journal:  Arch Neurol       Date:  1968-03

10.  Metachromatic leukodystrophy (MLD). IX. Qualitative and quantitative differences in urinary arylsulfatase A in different forms of MLD.

Authors:  D Stumpf; J Austin
Journal:  Arch Neurol       Date:  1971-02
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  3 in total

1.  Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy.

Authors:  J Kappler; R W Watts; E Conzelmann; D A Gibbs; P Propping; V Gieselmann
Journal:  Eur J Pediatr       Date:  1991-02       Impact factor: 3.183

2.  The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients.

Authors:  P Propping; W Friedl; M Huschka; K H Schlör; F Reimer; M Lee-Vaupel; E Conzelmann; K Sandhoff
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

3.  Phenotypic variation between siblings with Metachromatic Leukodystrophy.

Authors:  Saskia Elgün; Jakob Waibel; Christiane Kehrer; Diane van Rappard; Judith Böhringer; Stefanie Beck-Wödl; Jennifer Just; Ludger Schöls; Nicole Wolf; Ingeborg Krägeloh-Mann; Samuel Groeschel
Journal:  Orphanet J Rare Dis       Date:  2019-06-11       Impact factor: 4.123

  3 in total

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