Reuben Matalon, MD, PhD

  • 7166 Citations
  • 48 h-Index
1966 …2017

Research output per year

If you made any changes in Pure these will be visible here soon.

Research Output

Filter
Article
1985

Craniofacial and mucopolysaccharide abnormalities in Kniest dysplasia

Friede, H., Matalon, R., Harris, V. & Rosenthal, I. M., Dec 1 1985, In : Journal of Craniofacial Genetics and Developmental Biology. 5, 3, p. 267-276 10 p.

Research output: Contribution to journalArticle

9 Scopus citations

Folic acid responsive rages, seizures and homocystinuria

Murphy, J. V., Thome, L. M., Michals, K. & Matalon, R., Jun 1 1985, In : Journal of Inherited Metabolic Disease. 8, 2 Supplement, p. 109-110 2 p.

Research output: Contribution to journalArticle

6 Scopus citations

Infectious and Bleeding Complications in Patients With Glycogenosis lb

Ambruso, D. R., Mccabe, E. R. B., Anderson, D., Beaudet, A., Mahoney, D. H., Ballas, L. M., Brandt, I. K., Brown, B., Coleman, R., Kinney, T. R., Friedman, H. S., Falletta, J. M., Haymond, M. W., Simmons, P., Keating, J. P., Leonard, J. V., Dunger, D. B., Matalon, R., Roe, T. F. & Slonim, A. E., Jul 1985, In : American Journal of Diseases of Children. 139, 7, p. 691-697 7 p.

Research output: Contribution to journalArticle

74 Scopus citations

Phenylalanine metabolites, attention span and hyperactivity.

Michals, K. & Matalon, R., Aug 1 1985, In : American Journal of Clinical Nutrition. 42, 2, p. 361-365 5 p.

Research output: Contribution to journalArticle

12 Scopus citations

Return to diet therapy in patients with phenylketonuria

Michals, K., Dominik, M., Schuett, V., Brown, E. & Matalon, R., Jun 1985, In : The Journal of Pediatrics. 106, 6, p. 933-936 4 p.

Research output: Contribution to journalArticle

13 Scopus citations
1984

Biopterin synthesis defects: Problems in diagnosis

Hoganson, G., Berlow, S., Kaufman, S., Milstien, S., Schuett, V., Matalon, R., Naylor, E. & Seifert, W., Dec 1 1984, In : Pediatrics. 74, 6, p. 1004-1011 8 p.

Research output: Contribution to journalArticle

20 Scopus citations

Current status of biopterin screening

Matalon, R., Apr 1984, In : The Journal of Pediatrics. 104, 4, p. 579-581 3 p.

Research output: Contribution to journalArticle

19 Scopus citations

Gluconeogenic enzymes in the human placenta

Matalon, R. & Michals, K., Dec 1 1984, In : Journal of Inherited Metabolic Disease. 7, 4, p. 179-181 3 p.

Research output: Contribution to journalArticle

4 Scopus citations

Lipoamide dehydrogenase deficiency with primary lactic acidosis: Favorable response to treatment with oral lipoic acid

Matalon, R., Stumpf, D. A., Michals, K., Hart, R. D., Parks, J. K. & Goodman, S. I., Jan 1984, In : The Journal of Pediatrics. 104, 1, p. 65-69 5 p.

Research output: Contribution to journalArticle

51 Scopus citations

Treatment of the cbl B form of methylmalonic acidaemia with adenosylcobalamin

Batshaw, M. L., Thomas, G. H., Cohen, S. R., Matalon, R. & Mahoney, M. J., Jun 1 1984, In : Journal of Inherited Metabolic Disease. 7, 2, p. 65-68 4 p.

Research output: Contribution to journalArticle

9 Scopus citations
1983

Delayed dental age in hepatorenal glycogen storage disease.

Loevy, H. T., Matalon, R. & Rosenthal, I. M., Dec 1983, In : Journal of the American Dental Association (1939). 107, 6, p. 944-946 3 p.

Research output: Contribution to journalArticle

9 Scopus citations

Glucose-6-phosphatase as a marker for tumors of liver and kidney origin

Michals, K., Pringle, K., Pang, E. J. M. & Matalon, R., Aug 1983, In : Biochemical medicine. 30, 1, p. 127-130 4 p.

Research output: Contribution to journalArticle

4 Scopus citations

Hurler, Scheie, and Hurler-Scheie 'compound': Residual activity of α-l-iduronidase toward natural substrates suggesting allelic mutations

Matalon, R., Deanching, M. & Omura, K., Jun 1 1983, In : Journal of Inherited Metabolic Disease. 6, 2 Supplement, p. 133-134 2 p.

Research output: Contribution to journalArticle

6 Scopus citations

nonketonic hyperglycinemia: Treatment with diazepam - A competitor for glycine receptors

Matalon, R., Naidus, Hughes, J. R. & Michals, K., Jan 1 1983, In : Pediatrics. 71, 4, p. 581-584 4 p.

Research output: Contribution to journalArticle

24 Scopus citations
1982

Keratan and heparan sulfaturia: Glucosamine-6-sulfate sulfatase deficiency

Matalon, R., Wappner, R. & Deanching, M., Jan 1 1982, In : Annals of Clinical and Laboratory Science. 12, 3, p. 234-238 5 p.

Research output: Contribution to journalArticle

4 Scopus citations

Keratan and heparan sulphaturia: a mucopolysaccharidosis with an enzyme defect not previously identified

Matalon, R., Wappner, R., Deanching, M., Brandt, I. K. & Horwitz, A., Mar 1 1982, In : Journal of Inherited Metabolic Disease. 5, 1 Supplement, p. 57-58 2 p.

Research output: Contribution to journalArticle

2 Scopus citations

Lactic acidosis due to lipoamide dehydrogenase (LAD) deficiency: Improvement after oral lipoic acid

Matalon, R., Michals, K. & Hart, R., Jan 1 1982, In : Pediatric Research. 16, 4 II, p. No. 1090

Research output: Contribution to journalArticle

Screening for biopterin defects in newborns with phenylketonuria and other hyperphenylalaninemias

Matalon, R., Michals, K., Lee, C. L. & Nixon, J. C., Jan 1 1982, In : Annals of Clinical and Laboratory Science. 12, 5, p. 411-414 4 p.

Research output: Contribution to journalArticle

4 Scopus citations

Spontaneous chylothorax in Noonan's syndrome

Fisher, E., Weiss, E. B., Michals, K., DuBrow, I. W., Hastrieter, A. R. & Matalon, R., May 1 1982, In : European Journal of Pediatrics. 138, 3, p. 282-284 3 p.

Research output: Contribution to journalArticle

16 Scopus citations

The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in children

Matalon, R., Matthews, D. E., Michals, K. & Bier, D., Mar 1 1982, In : Journal of Inherited Metabolic Disease. 5, 1, p. 17-19 3 p.

Research output: Contribution to journalArticle

13 Scopus citations

Treatment of Inborn Errors of Urea Synthesis: Activation of Alternative Pathways of Waste Nitrogen Synthesis and Excretion

Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D. & 88 others, Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D., Schafer, I. A., Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D. & Schafer, I. A., Jun 10 1982, In : New England Journal of Medicine. 306, 23, p. 1387-1392 6 p.

Research output: Contribution to journalArticle

210 Scopus citations

Treatment of non-ketotic hyperglycinaemia with diazepam, choline and folic acid

Matalon, R., Michals, K., Naidu, S. & Hughes, J., Mar 1 1982, In : Journal of Inherited Metabolic Disease. 5, 1 Supplement, p. 3-5 3 p.

Research output: Contribution to journalArticle

7 Scopus citations
1981

Foamy Histiocytes in the CSF of a Patient With Infantile Niemann-Pick Disease

Chilcote, R. R., Miller, M., Dawson, G. & Matalon, R., Jan 1981, In : American Journal of Diseases of Children. 135, 1, p. 76-77 2 p.

Research output: Contribution to journalArticle

2 Scopus citations

Linguistic development of children with phenylketonuria and normal intelligence

Melnick, C. R., Michals, K. K. & Matalon, R., Feb 1981, In : The Journal of Pediatrics. 98, 2, p. 269-272 4 p.

Research output: Contribution to journalArticle

18 Scopus citations
1977

GLUCOSE-6-PHOSPHATASE ACTIVITY IN HUMAN PLACENTA: POSSIBLE DETECTION OF HETEROZYGOTE FOR GLYCOGEN-STORAGE DISEASE TYPE I

Matalon, R., Michals, K., Justice, P. & Deanching, M. N., Jun 25 1977, In : The Lancet. 309, 8026, p. 1360-1361 2 p.

Research output: Contribution to journalArticle

4 Scopus citations
1976

Allelic mutations in the mucopolysaccharidoses

Leisti, J., Rimoin, D. L., Kaback, M., Shapiro, L. J. & Matalon, R., Dec 1 1976, In : Birth Defects: Original Article Series. 12, 6, p. 81-91 11 p.

Research output: Contribution to journalArticle

4 Scopus citations

A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration

Newell, F. W., Matalon, R. & Meyer, S., Jan 1 1976, In : Transactions of the American Ophthalmological Society. Vol.73, p. 172-186 15 p.

Research output: Contribution to journalArticle

3 Scopus citations

Prenatal diagnosis of inborn errors of metabolism

Matalon, R., Jan 1 1976, In : International Journal of Gynecology and Obstetrics. 14, 4, p. 301-307 7 p.

Research output: Contribution to journalArticle

The enzymic defects in Morquio and Maroteaux-Lamy syndrome.

Dorfman, A., Arbogast, B. & Matalon, R., Jan 1 1976, In : Advances in experimental medicine and biology. 68, p. 261-276 16 p.

Research output: Contribution to journalArticle

23 Scopus citations

The mucopolysaccharidoses (A review)

Dorfman, A. & Matalon, R., Jan 1 1976, In : Proceedings of the National Academy of Sciences of the United States of America. 73, 2, p. 630-637 8 p.

Research output: Contribution to journalArticle

Open Access
95 Scopus citations
1975

A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration

Newell, F. W., Matalon, R. & Meyer, S., Sep 1975, In : American Journal of Ophthalmology. 80, 3 PART 1, p. 440-449 10 p.

Research output: Contribution to journalArticle

28 Scopus citations

Glycopeptide storage in skin fibroblasts cultured from a patient with α mannosidase deficiency

Chen Tsay, G., Dawson, G. & Matalon, R., Dec 1 1975, In : Journal of Clinical Investigation. 56, 3, p. 711-718 8 p.

Research output: Contribution to journalArticle

11 Scopus citations

Kniest syndrome with dominant inheritance and mucopolysacchariduria

Kim, H. J., Beratis, N. G., Brill, P., Raab, E., Hirschhorn, K. & Matalon, R., Dec 1 1975, In : American Journal of Human Genetics. 27, 6, p. 755-764 10 p.

Research output: Contribution to journalArticle

14 Scopus citations

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome

Shapira, E., DeGregorio, R. R., Matalon, R. & Nadler, H. L., Jan 20 1975, In : Biochemical and Biophysical Research Communications. 62, 2, p. 448-455 8 p.

Research output: Contribution to journalArticle

18 Scopus citations
1974

Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome

Matalon, R., Arbogast, B. & Dorfman, A., Dec 23 1974, In : Biochemical and Biophysical Research Communications. 61, 4, p. 1450-1457 8 p.

Research output: Contribution to journalArticle

50 Scopus citations

Excretion of mannose-rich complex carbohydrates by a patient with α-mannosidase deficiency (mannosidosis)

Tsay, G. C., Dawson, G. & Matalon, R., Jun 1974, In : The Journal of Pediatrics. 84, 6, p. 865-868 4 p.

Research output: Contribution to journalArticle

28 Scopus citations

Morquio's syndrome: Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase

Matalon, R., Arbogast, B., Justice, P., Brandt, I. K. & Dorfman, A., Nov 27 1974, In : Biochemical and Biophysical Research Communications. 61, 2, p. 759-765 7 p.

Research output: Contribution to journalArticle

86 Scopus citations

Sanfilippo A syndrome. Sulfamidase deficiency in cultured skin fibroblasts and liver

Matalon, R. & Dorfman, A., Jan 1 1974, In : Journal of Clinical Investigation. 54, 4, p. 907-912 6 p.

Research output: Contribution to journalArticle

Open Access
39 Scopus citations
1973
Open Access
12 Scopus citations

Cystic fibrosis: fractionation of fibroblast media demonstrating ciliary inhibition.

Bowman, B. H., Barnett, D. R., Matalon, R., Danes, B. S. & Bearn, A. G., Feb 1973, In : Proceedings of the National Academy of Sciences of the United States of America. 70, 2, p. 548-551 4 p.

Research output: Contribution to journalArticle

Open Access
53 Scopus citations

Hunter's syndrome: A deficiency of L-idurono-sulfate sulfatase

Sjöberg, I., Fransson, L. A., Matalon, R. & Dorfman, A., Oct 1 1973, In : Biochemical and Biophysical Research Communications. 54, 3, p. 1125-1132 8 p.

Research output: Contribution to journalArticle

51 Scopus citations

N-acetyl-β-hexosaminidase: Role in the degradation of glycosaminoglycans

Thompson, J. N., Stoolmiller, A. C., Matalon, R. & Dorfman, A., Jan 1 1973, In : Science. 181, 4102, p. 866-867 2 p.

Research output: Contribution to journalArticle

35 Scopus citations

Retinopathy in childhood dermatomyositis

Harrison, S. M., Frenkel, M., Grossman, B. J. & Matalon, R., Nov 1973, In : American Journal of Ophthalmology. 76, 5, p. 786-790 5 p.

Research output: Contribution to journalArticle

25 Scopus citations
1972

A CHEMICAL METHOD FOR THE ANTENATAL DIAGNOSIS OF MUCOPOLYSACCHARIDOSES

Matalon, R., Dorfman, A. & Nadler, H. L., Apr 8 1972, In : The Lancet. 299, 7754, p. 798-799 2 p.

Research output: Contribution to journalArticle

14 Scopus citations

Glycosphingolipids in cultured human skin fibroblasts. I. Characterization and metabolism in normal fibroblasts.

Dawson, G., Matalon, R. & Dorfman, A., Sep 25 1972, In : Journal of Biological Chemistry. 247, 18, p. 5944-5950 7 p.

Research output: Contribution to journalArticle

59 Scopus citations

Hurler's syndrome, an a-L-iduronidase deficiency

Matalon, R. & Dorfman, A., May 26 1972, In : Biochemical and Biophysical Research Communications. 47, 4, p. 959-964 6 p.

Research output: Contribution to journalArticle

74 Scopus citations
67 Scopus citations
1971

Gangliosides in Human Skin Fibroblasts and their Enrichment in the “Hurler Variant” and Krabbe's Disease

Hof, L., Matalon, R. & Dorfman, A., Jan 1 1971, In : Hoppe-Seyler's Zeitschrift fur Physiologische Chemie. 352, 2, p. 1329-1337 9 p.

Research output: Contribution to journalArticle

3 Scopus citations

Lactosylceramidosis: Lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts

Dawson, G., Matalon, R. & Stein, A. O., Sep 1971, In : The Journal of Pediatrics. 79, 3, p. 423-429 7 p.

Research output: Contribution to journalArticle

21 Scopus citations