Reuben Matalon, MD, PhD

  • 7166 Citations
  • 48 h-Index
1966 …2017

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1995

Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotype

Ohashi, T., Matalon, R., Barranger, J. A. & Eto, Y., Jan 1 1995, In : Gene Therapy. 2, 6, p. 363-368 6 p.

Research output: Contribution to journalArticle

8 Scopus citations

Prenatal diagnosis for Canavan disease: the use of DNA markers

Matalon, R., Kaul, R., Gao, G. P., Michals, K., Gray, R. G. F., Bennett-Briton, S., Norman, A., Smith, M. & Jakobs, C., Mar 1 1995, In : Journal of Inherited Metabolic Disease. 18, 2, p. 215-217 3 p.

Research output: Contribution to journalArticle

14 Scopus citations
1994

Canavan disease

Verdura, C., Perez-Pascual, S. R. & Matalon, R., Jan 1 1994, In : International Pediatrics. 9, 3, p. 221-223 3 p.

Research output: Contribution to journalArticle

Canavan disease: Mutations among Jewish and non-Jewish patients

Kaul, R., Gao, G. P., Aloya, M., Balamurugan, K., Petrosky, A., Michals, K. & Matalon, R., Jul 19 1994, In : American Journal of Human Genetics. 55, 1, p. 34-41 8 p.

Research output: Contribution to journalArticle

106 Scopus citations

Canavan disease: Molecular basis of aspartoacylase deficiency

Kaul, R., Gao, G. P., Balamurugan, K. & Matalon, R., May 1 1994, In : Journal of Inherited Metabolic Disease. 17, 3, p. 295-297 3 p.

Research output: Contribution to journalArticle

10 Scopus citations

Canavan Disease: Genomic Organization and Localization of Human ASPA to 17p13-ter and Conservation of the ASPA Gene during Evolution

Kaul, R., Balamurugan, K., Gao, G. P. & Matalon, R., May 15 1994, In : Genomics. 21, 2, p. 364-370 7 p.

Research output: Contribution to journalArticle

52 Scopus citations

Frequency of 12 mutations in 114 children with phenylketonuria in the Midwest region of the USA

Kaul, R., Matalon, R., Allen, R., Fisch, R. O., Michals, K., Petrosky, A. & Sullivan, D., May 1 1994, In : Journal of Inherited Metabolic Disease. 17, 3, p. 356-358 3 p.

Research output: Contribution to journalArticle

5 Scopus citations

Maternal PKU Collaborative Study: Pregnancy outcome and postnatal head growth

Matalon, R., Michals, K., Azen, C., Friedman, E., Koch, R., Rouse, B., Hanley, W. B. & de la Cruz, F., May 1 1994, In : Journal of Inherited Metabolic Disease. 17, 3, p. 353-355 3 p.

Research output: Contribution to journalArticle

4 Scopus citations

The international collaborative study of maternal phenylketonuria: status report 1994

Koch, R., Levy, HL., Matalon, R., Rouse, B., Hanley, WB., Trefz, F., Azen, C., Friedan, EG., de la Cruz, F., Güttler, F. & Acosta, PB., Dec 1994, In : Acta Pædiatrica. 83, p. 111-119 9 p.

Research output: Contribution to journalArticle

38 Scopus citations

The international collaborative study of maternal phenylketonuria: Status report 1994

Koch, R., Levy, H. L., Matalon, R., Rouse, B., Hanley, W. B., Trefz, F., Azen, C. & Friedman, E. G., 1994, In : Acta Paediatrica, International Journal of Paediatrics, Supplement. 83, 407, p. 111-119 9 p.

Research output: Contribution to journalArticle

1 Scopus citations

The North American collaborative study of maternal phenylketonuria: Status report, 1993

Koch, R., Levy, H. L., Matalon, R., Rouse, B., Hanley, W. & Azen, C., 1994, In : Obstetrical and Gynecological Survey. 49, 6, p. 377-378 2 p.

Research output: Contribution to journalArticle

1993

Canavan disease: Biochemical and molecular studies

Matalon, R., Kaul, R. & Michals, K., Jul 1 1993, In : Journal of Inherited Metabolic Disease. 16, 4, p. 744-752 9 p.

Research output: Contribution to journalArticle

44 Scopus citations

Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease

Kaul, R., Gao, G. P., Balamurugan, K. & Matalon, R., Oct 1993, In : Nature Genetics. 5, 2, p. 118-123 6 p.

Research output: Contribution to journalArticle

174 Scopus citations

Elevated serum sialic acid in idiopathic acute iridocyclitis

Lam, S., Tessler, H. H., Farber, M. D., Matalon, R., Deaching, M. N., Rychlik, D. S. & Lam, B. L., Feb 1993, In : Acta Ophthalmologica. 71, 1, p. 119-121 3 p.

Research output: Contribution to journalArticle

1 Scopus citations

Malonic aciduria and cardiomyopathy

Matalon, R., Michaels, K., Kaul, R., Whitman, V., Rodriguez-Novo, J., Goodman, S. & Thorburn, D., May 1 1993, In : Journal of Inherited Metabolic Disease. 16, 3, p. 571-573 3 p.

Research output: Contribution to journalArticle

38 Scopus citations

Prospective management of a child with neonatal citrullinemia

Melnyk, A. R., Matalon, R., Henry, B. W., Zeller, W. P. & Lange, C., Jan 1993, In : The Journal of Pediatrics. 122, 1, p. 96-98 3 p.

Research output: Contribution to journalArticle

9 Scopus citations

The Effect of Nutrient Intake on Pregnancy Outcome in Maternal Phenylketonuria

KOCH, RICHARD., WENZ, ELIZABETH., AZEN, COLLEEN., FRIEDMAN, EVA. G., LEVY, HARVEY., ROHR, FRANCES., ROUSE, BOBBYE., CASTIGLIONI, LOIS., MATALON, REUBEN., MICHALS‐MATALON, KIMBERLEE., HANLEY, WILLIAM., AUSTIN, VALERIE., de LA CRUZ, FELIX. & ACOSTA, PHYLLIS. B., Mar 1993, In : Annals of the New York Academy of Sciences. 678, 1, p. 348-349 2 p.

Research output: Contribution to journalArticle

2 Scopus citations

The North American Collaborative Study of Maternal Phenylketonuria: Status Report 1993

Koch, R., Levy, H. L., Matalon, R., Rouse, B., Hanley, W. & Azen, C., Nov 1993, In : American Journal of Diseases of Children. 147, 11, p. 1224-1230 7 p.

Research output: Contribution to journalArticle

48 Scopus citations

The North American collaborative study of maternal phenylketonuria (PKU)

Koch, R., Levy, H. L., Matalon, R., Rouse, B., Hanley, W., Friedman, E. G., Azen, C. & De la Cruz, F., Jan 1 1993, In : International Pediatrics. 8, 1, p. 89-96 8 p.

Research output: Contribution to journalArticle

3 Scopus citations
1992

A Treatment Program for Adolescents With Phenylketonuria

Gleason, L. A., Michals, K., Matalon, R., Langenberg, P. & Kamath, S., Jun 1992, In : Clinical pediatrics. 31, 6, p. 331-335 5 p.

Research output: Contribution to journalArticle

24 Scopus citations
7 Scopus citations

Maternal phenylketonuria collaborative study, obstetric aspects and outcome: The first 6 years

Matalon, R., de la Cruz, F., Azen, C. & Walla, C. A., Jan 1 1992, In : American journal of obstetrics and gynecology. 166, 4, p. 1150-1162 13 p.

Research output: Contribution to journalArticle

56 Scopus citations

Prenatal diagnosis of canavan disease

Matalon, R., Michals, K., Gashkoff, P. & Kaul, R., May 1 1992, In : Journal of Inherited Metabolic Disease. 15, 3, p. 392-394 3 p.

Research output: Contribution to journalArticle

22 Scopus citations
1991

Children of fathers with phenylketonuria: An international survey

Fisch, R. O., Matalon, R., Weisberg, S. & Michals, K., May 1991, In : The Journal of Pediatrics. 118, 5, p. 739-741 3 p.

Research output: Contribution to journalArticle

5 Scopus citations

Defects in the oxidation of fatty acids

Matalon, R., Michals, K. & Kaul, R., Jan 1 1991, In : International Pediatrics. 6, 2, p. 126-128 3 p.

Research output: Contribution to journalArticle

Intellectual Development in 12-Year-Old Children Treated for Phenylketonuria

Azen, C. G., Koch, R., Friedman, E. G., Berlow, S., Coldwell, J., Krause, W., Matalon, R., McCabe, E., O'Flynn, M., Peterson, R., Rouse, B., Scott, C. R., Sigman, B., Valle, D. & Warner, R., Jan 1991, In : American Journal of Diseases of Children. 145, 1, p. 35-39 5 p.

Research output: Contribution to journalArticle

103 Scopus citations

Maternal PKU collaborative study: the effect of nutrient intake on pregnancy outcome

Matalon, R., Michals, K., Azen, C., Friedman, E. G., Koch, R., Wenz, E., Levy, H., Rohr, F., Rouse, B., Castiglioni, L., Hanley, W., Austin, V. & de la Cruz, F., May 1 1991, In : Journal of Inherited Metabolic Disease. 14, 3, p. 371-374 4 p.

Research output: Contribution to journalArticle

10 Scopus citations

Phenylketonuria: screening, treatment and maternal PKU

Matalon, R. & Michals, K., Aug 1991, In : Clinical Biochemistry. 24, 4, p. 337-342 6 p.

Research output: Contribution to journalArticle

17 Scopus citations

Purification, Characterization, and Localization of Aspartoacylase from Bovine Brain

Kaul, R., Casanova, J., Johnson, A. B., Tang, P. & Matalon, R., Jan 1991, In : Journal of neurochemistry. 56, 1, p. 129-135 7 p.

Research output: Contribution to journalArticle

91 Scopus citations
1990

A preliminary report of the collaborative study of maternal phenylketonuria in the United States and Canada

Koch, R., Hanley, W., Levy, H., Matalon, R., Rouse, B., Cruz, F. D., Azen, C. & Friedman, E. G., Jul 1 1990, In : Journal of Inherited Metabolic Disease. 13, 4, p. 641-650 10 p.

Research output: Contribution to journalArticle

35 Scopus citations

Maternal phenylketonuria pregnancy outcome: a preliminary report of facial dysmorphology and major malformations

Rouse, B., Lockhart, L., Matalon, R., Azen, C., Koch, R., Hanley, W., Levy, H., dela Cruz, F. & Friedman, E., May 1 1990, In : Journal of Inherited Metabolic Disease. 13, 3, p. 289-291 3 p.

Research output: Contribution to journalArticle

36 Scopus citations

Ocular histopathology and ultrastructure of Morquio syndrome (systemic mucopolysaccharidosis IV A)

Iwamoto, M., Nawa, Y., Maumenee, I. H., Young-Ramsaran, J., Matalon, R. & Green, W. R., Jul 1 1990, In : Graefe's Archive for Clinical and Experimental Ophthalmology. 228, 4, p. 342-349 8 p.

Research output: Contribution to journalArticle

23 Scopus citations

Plasma amino acid patterns in very low birth weight infants during parenteral nutrition

Srinivasan, G., Amin, A., Pildes, R. S., Lilien, L. D. & Matalon, R., Jan 1 1990, In : The Indian Journal of Pediatrics. 57, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

3 Scopus citations

Transmission of ring 14 chromosome from mother to two sons

Matalon, R., Supple, P., Wyandt, H. & Rosenthal, I. M., Aug 3 1990, In : American Journal of Medical Genetics. 36, 4, p. 381-385 5 p.

Research output: Contribution to journalArticle

14 Scopus citations
1989

Aspartoacylase Deficiency: The Enzyme Defect in Canavan Disease

Matalon, R., Kaul, R., Casanova, J., Michals, K., Johnson, A., Rapin, I., Gashkoff, P. & Deanching, M., Apr 1989, In : Journal of Inherited Metabolic Disease. 12, 2, p. 329-331 3 p.

Research output: Contribution to journalArticle

75 Scopus citations

Effects of ascorbic acid in alkaptonuria: Alterations in benzoquinone acetic acid and an ontogenic effect in infancy

Wolff, J. A., Barshop, B., Nyhan, W. L., Leslie, J., Seegmiller, J. E., Gruber, H., Garst, M., Winter, S., Michals, K. & Matalon, R., Aug 1989, In : Pediatric Research. 26, 2, p. 140-144 5 p.

Research output: Contribution to journalArticle

Open Access
74 Scopus citations
1988

Analysis of the pentafluorobenzoyl derivative of phenylethylamine utilizing negative ion chemical ionization and gas chromatography/mass spectrometry

Gashkoff, P., Matalon, R., Papa, V. & Sebasta, D., Oct 1988, In : Biological Mass Spectrometry. 16, 1-12, p. 327-329 3 p.

Research output: Contribution to journalArticle

5 Scopus citations

Aspartoacyclase deficiency and N-acetylaspartic aciduria in patients with Canavan disease

Matalon, R., Michals, K., Sebesta, D., Deanching, M., Gashkoff, P. & Casanova, J., Jan 1 1988, In : American Journal of Medical Genetics. 29, 2, p. 463-471 9 p.

Research output: Contribution to journalArticle

297 Scopus citations

Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative Study

Michals, K., Azen, C., Acosta, P., Koch, R. & Matalon, R., Jan 1 1988, In : Journal of the American Dietetic Association. 88, 10, p. 1226-1229 4 p.

Research output: Contribution to journalArticle

30 Scopus citations

Carrier detection for sanfilippo A syndrome

Matalon, R., Deanching, M., Marback, R. & Michals, K., Jun 1 1988, In : Journal of Inherited Metabolic Disease. 11, 2, p. 158-160 3 p.

Research output: Contribution to journalArticle

9 Scopus citations

Isovaleric acidaemia in a premature infant: Diagnosis and treatment

Heimler, R., Hennes, H., Khayata, S., Sasidharan, P. & Matalon, R., Sep 1 1988, In : Journal of Inherited Metabolic Disease. 11, 3, p. 313-314 2 p.

Research output: Contribution to journalArticle

Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuria

Michals, K., Lopus, M. & Matalon, R., Feb 1988, In : Biochemical Medicine and Metabolic Biology. 39, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

12 Scopus citations

Simpson-Golabi-Behmel syndrome: Follow-up of the Michigan family

Opitz, J. M., Herrmann, J., Gilbert, E. F. & Matalon, R., Jan 1 1988, In : American Journal of Medical Genetics. 30, 1-2, p. 301-308 8 p.

Research output: Contribution to journalArticle

20 Scopus citations
1987

Dominant inheritance of a syndrome similar to Rubinstein-Taybi

Cotsirilos, P., Taylor, J. C. & Matalon, R., Jan 1 1987, In : American Journal of Medical Genetics. 26, 1, p. 85-93 9 p.

Research output: Contribution to journalArticle

21 Scopus citations

Phenotypic Features of Patients With Congenital Adrenal Hypoplasia and Glycerol Kinase Deficiency

Wise, J. E., Matalon, R., Morgan, A. M. & McCabe, E. R. B., Jul 1987, In : American Journal of Diseases of Children. 141, 7, p. 744-747 4 p.

Research output: Contribution to journalArticle

28 Scopus citations
1986

Galactokinase Activity in Patients with Idiopathic Cataracts

Elman, M. J., Miller, M. T. & Matalon, R., Jan 1 1986, In : Ophthalmology. 93, 2, p. 210-215 6 p.

Research output: Contribution to journalArticle

7 Scopus citations

Maternal PKU: Strategies for Dietary Treatment and Monitoring Compliance

MATALON, REUBEN., MICHALS, KIMBERLEE. & GLEASON, LINDA., Dec 1986, In : Annals of the New York Academy of Sciences. 477, 1, p. 223-230 8 p.

Research output: Contribution to journalArticle

9 Scopus citations

Phenylalanine meta10545tes in treated phenylketonuric children

Michals, K., Lopus, M., Gashkoff, P. & Matalon, R., Jun 1 1986, In : Journal of Inherited Metabolic Disease. 9, 2 Supplement, p. 212-214 3 p.

Research output: Contribution to journalArticle

4 Scopus citations

Sanfilippo disease in Greece

Beratis, N. G., Sklower, S. L., Wilbur, L. & Matalon, R., Feb 1986, In : Clinical Genetics. 29, 2, p. 129-132 4 p.

Research output: Contribution to journalArticle

13 Scopus citations
1985

A therapeutic trial of amniotic epithelial cell implantation in patients with lysosomal storage diseases

Yeager, A. M., Singer, H. S., Buck, J. R., Matalon, R., Brennan, S., O'Toole, S. O. & Moser, H. W., Dec 1 1985, In : American Journal of Medical Genetics. 22, 2, p. 347-355 9 p.

Research output: Contribution to journalArticle

44 Scopus citations