Reuben Matalon, MD, PhD

  • 7166 Citations
  • 48 h-Index
1966 …2017

Research output per year

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Research Output

1999

Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: Report from the maternal phenylketonuria collaborative study

Güttler, F., Azen, C., Guldberg, P., Romstad, A., Hanley, W. B., Levy, H. L., Matalon, R., Rouse, B. M., Trefz, F., De La Cruz, F. & Koch, R., Aug 1 1999, In : Pediatrics. 104, 2 I, p. 258-262 5 p.

Research output: Contribution to journalArticle

52 Scopus citations

The International Collaborative Study of Maternal Phenylketonuria Status Report 1998

Koch, R., Friedman, E., Azen, C., Hanley, W., Levy, H., Matalon, R., Rouse, B., Trefz, F., Waisbren, S., Michals-Matalon, K., Acosta, P., Güttler, F., Ullrich, K., Platt, L. & De La Cruz, F., Jun 8 1999, In : Mental Retardation and Developmental Disabilities Research Reviews. 5, 2, p. 117-121 5 p.

Research output: Contribution to journalArticle

9 Scopus citations
1998

A novel mutation in the switch 3 region of G(s)α in a patient with albright hereditary osteodystrophy impairs GDP binding and receptor activation

Warner, D. R., Weng, G., Yu, S., Matalon, R. & Weinstein, L. S., Sep 11 1998, In : Journal of Biological Chemistry. 273, 37, p. 23976-23983 8 p.

Research output: Contribution to journalArticle

55 Scopus citations

Fuzzy clustering of vitamin and homocysteine levels in patients with history of ischemic stroke

Dickerson, J. A., Matalon, R. & Helgason, C., Jan 1 1998, 1998 Conference of the North American Fuzzy Information Processing Society, NAFIPS 1998. Hall, L. O. & Bezdek, J. (eds.). Institute of Electrical and Electronics Engineers Inc., p. 231-236 6 p. (Annual Conference of the North American Fuzzy Information Processing Society - NAFIPS).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

3 Scopus citations

Molecular basis of Canavan disease

Matalon, R. & Michals-Matalon, K., Jan 1 1998, In : European Journal of Paediatric Neurology. 2, 2, p. 69-76 8 p.

Research output: Contribution to journalReview article

24 Scopus citations

Neonatal neurological assessment of offspring in maternal phenylketonuria

Waisbren, S. E., Chang, P., Levy, H. L., Shifrin, H., Allred, E., Azen, C., De La Cruz, F., Hanley, W., Koch, R., Matalon, R. & Rouse, B., Feb 6 1998, In : Journal of Inherited Metabolic Disease. 21, 1, p. 39-48 10 p.

Research output: Contribution to journalArticle

21 Scopus citations

Spongy degeneration of the brain, Canavan disease: Biochemical and molecular findings

Matalon, R. & Michals-Matalon, K., Dec 1 1998, In : Pediatric Pathology and Molecular Medicine. 18, 6, p. 471-481 11 p.

Research output: Contribution to journalArticle

1 Scopus citations

Spongy degeneration of the brain, Canavan disease: Biochemical and molecular findings

Matalon, R. & Michals-Matalon, K., Dec 1 1998, In : Fetal and Pediatric Pathology. 18, 6, p. 471-481 11 p.

Research output: Contribution to journalArticle

2 Scopus citations

Sulfamidase deficiency in a family of dachshunds: A canine model of mucopolysaccharidosis IIIA (Sanfilippo A)

Fischer, A., Carmichael, K. P., Munnell, J. F., Jhabvala, P., Thompson, J. N., Matalon, R., Jezyk, P. F., Wang, P. & Giger, U., Jul 1998, In : Pediatric Research. 44, 1, p. 74-82 9 p.

Research output: Contribution to journalArticle

Open Access
45 Scopus citations
1997

Canavan disease: Diagnosis and molecular analysis

Matalon, R., Jun 1 1997, In : Genetic Testing. 1, 1, p. 21-25 5 p.

Research output: Contribution to journalArticle

23 Scopus citations

Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen

Byers, P. H., Duvic, M., Atkinson, M., Robinow, M., Smith, L. T., Krane, S. M., Greally, M. T., Ludman, M., Matalon, R., Pauker, S., Quanbeck, D. & Schwarze, U., Oct 3 1997, In : American Journal of Medical Genetics. 72, 1, p. 94-105 12 p.

Research output: Contribution to journalArticle

74 Scopus citations

Galactosemia: Promise, frustration and challenge

Matalon, R., Jun 1 1997, In : Journal of the American College of Nutrition. 16, 3, p. 190-191 2 p.

Research output: Contribution to journalArticle

2 Scopus citations

Maternal phenylketonuria collaborative study (MPKUCS) offspring: Facial anomalies, malformations, and early neurological sequelae

Rouse, B., Azen, C., Koch, R., Matalon, R., Hanley, W., De La Cruz, F., Trefz, F., Friedman, E. & Shifrin, H., Mar 3 1997, In : American Journal of Medical Genetics. 69, 1, p. 89-95 7 p.

Research output: Contribution to journalArticle

83 Scopus citations

Phenylketonuria: Current dietary treatment practices in the United States and Canada

Fisch, R. O., Matalon, R., Weisberg, S. & Michals, K., Apr 1 1997, In : Journal of the American College of Nutrition. 16, 2, p. 147-151 5 p.

Research output: Contribution to journalArticle

29 Scopus citations

Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome

Jaquez, M., Driscoll, D. A., Li, M., Emanuel, B. S., Hernandez, I., Jaquez, F., Lembert, N., Ramirez, J. & Matalon, R., May 2 1997, In : American Journal of Medical Genetics. 70, 1, p. 6-10 5 p.

Research output: Contribution to journalArticle

18 Scopus citations
1996

Canavan disease

Matalon, R., Jan 1 1996, In : Molecular and Chemical Neuropathology. 27, 1, p. 54-57 4 p.

Research output: Contribution to journalArticle

1 Scopus citations

Fragile X syndrome in two siblings with major congenital malformations

Giampietro, P. F., Haas, B. R., Lipper, E., Gutman, A., Zellers, N. J., LaTrenta, G. S., Sklower Brooks, S., Matalon, R., Kaul, R., Ding, X. H. & Brown, W. T., May 17 1996, In : American Journal of Medical Genetics. 63, 2, p. 396-400 5 p.

Research output: Contribution to journalArticle

2 Scopus citations

Gene therapy for metachromatic leukodystrophy

Ohashi, T., Watabe, K., Sato, Y., Saito, I., Barranger, J. A., Matalon, R. & Eto, Y., Apr 1996, In : Pediatrics International. 38, 2, p. 193-201 9 p.

Research output: Contribution to journalArticle

5 Scopus citations

Identification and expression of eight novel mutations among non-Jewish patients with Canavan disease

Kaul, R., Gao, G. P., Matalon, R., Aloya, M., Su, Q., Jin, M., Johnson, A. B., Schutgens, R. B. H. & Clarke, J. T. R., Jun 27 1996, In : American Journal of Human Genetics. 59, 1, p. 95-102 8 p.

Research output: Contribution to journalArticle

56 Scopus citations

Maternal non-phenylketonuric mild hyperphenylalaninemia

Levy, H. L., Waisbren, S. E., Lobbregt, D., Allred, E., Leviton, A., Koch, R., Hanley, W. B., Rouse, B., Matalon, R. & de la Cruz, F., Jan 1 1996, In : European Journal of Pediatrics. 155, 1 Supplement

Research output: Contribution to journalArticle

11 Scopus citations

Phenylalanine hydroxylase gene mutations in the United States: Report from the Maternal PKU Collaborative Study

Guldberg, P., Levy, H. L., Hanley, W. B., Koch, R., Matalon, R., Rouse, B. M., Trefz, F., De la Cruz, F., Henriksen, K. F. & Guttler, F., Jun 27 1996, In : American Journal of Human Genetics. 59, 1, p. 84-94 11 p.

Research output: Contribution to journalArticle

76 Scopus citations

The MRI suggests a leukodystrophy, but tests are negative - What should we do? Probing white-matter disorders

Tager, J. M., Moser, H. W., Barker, P. B., Barth, P. G., Boltshauser, E., Campagnoni, A. T., Dawson, G., DeVivo, D. C., Federico, A., Fluharty, A. L., Gieselmann, V., Hodes, M. E., Hurko, O., Jaeken, J., Kruse, B., Matalon, R., Matthieu, J. M., Naidu, S. & Powers, J. M., Feb 20 1996, In : Molecular and Chemical Neuropathology. 27, 1, p. 1-106 106 p.

Research output: Contribution to journalArticle

1995

Canavan disease: From spongy degeneration to molecular analysis

Matalon, R., Michals, K. & Kaul, R., Oct 1995, In : The Journal of Pediatrics. 127, 4, p. 511-517 7 p.

Research output: Contribution to journalArticle

98 Scopus citations

Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency

Ichinose, H., Ohye, T., Matsuda, Y., Hori, T. A., Blau, N., Burlina, A., Rouse, B., Matalon, R., Fujita, K. & Nagatsu, T., Jan 1 1995, In : Journal of Biological Chemistry. 270, 17, p. 10062-10071 10 p.

Research output: Contribution to journalArticle

Open Access
133 Scopus citations

Genomic Organization of Mouse and Human GTP Cyclohydrolase I Genes and Mutations Found in the Human Gene

Ichinose, H., Blau, N., Matalont, R. & Nagatsu, T., Aug 1995, In : Pteridines. 6, 3, p. 104-107 4 p.

Research output: Contribution to journalArticle

1 Scopus citations

Novel (cys152>arg) missense mutation in an Arab patient with Canavan disease

Kaul, R., Gao, G. P., Michals, K., Whelan, D. T., Levin, S. & Matalon, R., 1995, In : Human mutation. 5, 3, p. 269-271 3 p.

Research output: Contribution to journalArticle

23 Scopus citations

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: 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

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: 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

Introduction

Matalon, R., Jan 1 1994, In : International Pediatrics. 9, 3, 1 p.

Research output: Contribution to journalEditorial

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

Editorial

Matalon, R., Jan 1 1993, In : International Pediatrics. 8, 1, 1 p.

Research output: Contribution to journalEditorial

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