Access the full text.
Sign up today, get DeepDyve free for 14 days.
J. Warner (1975)
Juvenile onset metachromatic leucodystrophy. Failure of response on a low vitamin A diet.Archives of Disease in Childhood, 50
J. Austin, D. Armstrong, L. Shearer, D. McAfee (1966)
Metachromatic form of diffuse cerebral sclerosis. VI. A rapid test for the sulfatase A deficiency in metachromatic leukodystrophy (MLD) urine.Archives of neurology, 14 3
La Veck GD Hain RF (1958)
Metachromatic leuko-encephalopathyPediatrics, 22
Clausen J Melchior JC (1968)
Metachromatic leucodystrophy in early childhood: Treatment with a diet deficient in vitamin AActa Paediatr Scand, 57
A. Percy, R. Brady (1968)
Metachromatic Leukodystrophy: Diagnosis with Samples of Venous BloodScience, 161
J. Austin (1959)
Metachromatic Sulfatides in Cerebral White Matter and Kidney.∗Proceedings of the Society for Experimental Biology and Medicine, 100
Sato K Matsukura T (1958)
A study on the winding direction of fingerprint pattern in twinsShikoku Acta Med, 12
Nyberg-Hansen R (1972)
Metachromatic leukodystrophy: Two unusual cases of the late infantile formZ Neurol, 203
Dodgson KS Baum H (1959)
The assay of arylsulfatase A and B in human urineClin Chim Acta, 4
J. Singh, D. Tavella, N. Ferrante (1975)
Measurements of arylsulfatases A and B in human serum.The Journal of pediatrics, 86 4
N. Beratis, A. Aaron, K. Hirschhorn (1973)
Metachromatic leukodystrophy: detection in serum.The Journal of pediatrics, 83 5
H. Jatzkewitz (1958)
Zwei Typen von Cerebrosid-schwefelsäureestern als sog. „Prälipoide“ und Speichersubstanzen bei der Leukodystrophie, Typ Scholz (metachromatische Form der diffusen Sklerose)Biological Chemistry, 311
Roger Snyder, Roscoe Brady (1969)
The use of white cells as a source of diagnostic material for lipid storage diseases.Clinica chimica acta; international journal of clinical chemistry, 25 2
R. Hain, G. Laveck (1958)
Metachromatic leuko-encephalopathy; review with illus-trative case report.Pediatrics, 22 6
M. Porter, A. Fluharty, H. Kihara (1969)
Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.Proceedings of the National Academy of Sciences of the United States of America, 62 3
J. Austin, D. Armstrong, L. Shearer (1965)
Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD).Archives of neurology, 13 6
J. Melchior, J. Clausen (1968)
METACHROMATIC LEUCODYSTROPHY IN EARLY CHILDHOOD Treatment with a diet deficient in vitamin AActa Pædiatrica, 57
Jatzkewitz H (1958)
Zwei Typen von Cerebrocid-Schwefelsäureestern als sog: "Prälipoide" und speichersubstanzen bei der Leukodystrophie, Typ Scholz (metachromatische Form der diffusen Sklerose)Z Physiol Chem, 311
Matsukura T (1952)
Studies on the inheritance of fingerprints (report 3): On the inheritance of the quantity of papillary ridgesShikoku Acta Med, 3
Ogawa K (1961)
Late infantile metachromatic leukodystrophyArch Neurol, 4
Taniguchi Noboru, N. Ichiro (1970)
Enzymatic abnormality of the carrier state in metachromatic leukodystrophyClinica Chimica Acta, 29
R. Allen, J. Mccusker, W. Tourtellotte (1962)
Metachromatic leukodystrophy: clinical, histochemical, and cerebrospinal fluid abnormalities.Pediatrics, 30
L. Działoszyński, J. Gniot-Szulż, ycka (1967)
Some clinical aspects of arylsulphatase activityClinica Chimica Acta, 15
Abstract • Arylsulfatase A (ASA) activity in urine and serum was assayed on two 21-monthold monozygotic twins with presumed metachromatic leukodystrophy (MLD), their parents, and kin. The patients showed a marked reduction in ASA activity in both urine and serum. The twins' parents and 11 kin, a total of 13 persons, were examined for ASA activity in serum, but it was not possible to delineate heterozygous carriers of MLD by the present study. The assay of ASA activity in serum promises to be useful for diagnosis of MLD. References 1. Hain RF, La Veck GD: Metachromatic leuko-encephalopathy . Pediatrics 22:1064-1073, 1958. 2. Ogawa K: Late infantile metachromatic leukodystrophy . Arch Neurol 4:418-429, 1961.Crossref 3. Allen RJ, McCusker JJ, Tourtellote WW: Metachromatic leukodystrophy: Clinical, histochemical and cerebrospinal fluid abnormalities . Pediatrics 30:629-638, 1962. 4. Nyberg-Hansen R: Metachromatic leukodystrophy: Two unusual cases of the late infantile form . Z Neurol 203:145-154, 1972. 5. Warner JO: Juvenile onset metachromatic leukodystrophy: Failure of response on a low vitamin A diet . Arch Dis Child 50:735-737, 1975.Crossref 6. Beratis NG, Aron AM, Hirschhorn K: Metachromatic leukodystrophy: Detection in serum . J Pediatr 83:824-827, 1973.Crossref 7. Singh J, Tavella D, Di Ferrante N: Measurements of arylsulfatases A and B in human serum . J Pediatr 86:574-576, 1975.Crossref 8. Matsukura T, Sato K, Terauchi H: A study on the winding direction of fingerprint pattern in twins . Shikoku Acta Med 12:414-419, 1958. 9. Matsukura T: Studies on the inheritance of fingerprints (report 3): On the inheritance of the quantity of papillary ridges . Shikoku Acta Med 3:108-119, 1952. 10. Baum H, Dodgson KS, Spencer B: The assay of arylsulfatase A and B in human urine . Clin Chim Acta 4:453-455, 1959.Crossref 11. Taniguchi N, Nanba I: Enzymatic abnormality of carrier state in metachromatic leukodystrophy . Clin Chim Acta 29:375-379, 1970.Crossref 12. Jatzkewitz H: Zwei Typen von Cerebrocid-Schwefelsäureestern als sog: "Prälipoide" und speichersubstanzen bei der Leukodystrophie, Typ Scholz (metachromatische Form der diffusen Sklerose) . Z Physiol Chem 311:279-282, 1958.Crossref 13. Austin JH: Metachromatic sulfatides in cerebral white matter and kidney . Proc Soc Exp Biol Med 100:361-364, 1959.Crossref 14. Austin J, Armstrong D, Shearer L: Metachromatic form of diffuse cerebral sclerosis: V. The nature and significance of low sulfatase activity: A controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD) . Arch Neurol 13:593-614, 1965.Crossref 15. Austin J, Armstrong D, Shearer L, McAfee D: Metachromatic form of diffuse sclerosis: VI. A rapid test for the sulfate A deficiency in metachromatic leukodystrophy (MLD) urine . Arch Neurol 14:259-269, 1966.Crossref 16. Percy AL, Brady RO: Metachromatic leukodystrophy: Diagnosis with samples of venous blood . Science 161:594-595, 1968.Crossref 17. Porter MT, Fluharty AL, Kihara H: Metachromatic leukodystrophy: Arylsulfatase A deficiency in skin fibroblast cultures . Proc Natl Acad Sci USA 62:887-891, 1969.Crossref 18. Djialoszynski LM, Gniot-Szulzycka J: Some clinical aspects of arylsulfatase activity . Clin Chim Acta 15:381-386, 1967.Crossref 19. Melchior JC, Clausen J: Metachromatic leucodystrophy in early childhood: Treatment with a diet deficient in vitamin A . Acta Paediatr Scand 57:2-8, 1968.Crossref 20. Snyder RA, Brady RO: The use of white cells as a source of diagnostic material for lipid storage disease . Clin Chim Acta 25:331-338, 1969.Crossref
Archives of Neurology – American Medical Association
Published: Oct 1, 1978
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.