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R Matalon

Showing results (111-120 of 185) with videos related to

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Nephron|January 1, 1974
Hemodialysis using femoral vessel cannulationB D Nidus, R Matalon, L A Katz, et al.
American Journal of Human Genetics|July 1, 1994
Canavan disease: mutations among Jewish and non-Jewish patientsR Kaul, G P Gao, M Aloya, et al.
The Journal of Infectious Diseases|December 1, 1971
The use of gentamicin in peritoneal dialysis. II. Microbiologic and clinical resultsP J Hyams, T Smithivas, R Matalon, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Malonic aciduria and cardiomyopathyR Matalon, K Michaels, R Kaul, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1996
Gene therapy for metachromatic leukodystrophyT Ohashi, K Watabe, Y Sato, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Frequency of 12 mutations in 114 children with phenylketonuria in the Midwest region of the USAR Kaul, R Matalon, R Allen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1990
Ocular histopathology and ultrastructure of Morquio syndrome (systemic mucopolysaccharidosis IV A)M Iwamoto, Y Nawa, I H Maumenee, et al.
European Journal of Pediatrics|July 1, 1996
Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994R Koch, H Levy, W Hanley, et al.
Molecular Genetics and Metabolism Reports|October 20, 2025
Carbonic anhydrase VA deficiency due to a novel <i>CA5A</i> variantLaura Keehan, Elizabeth Null, Lekha Chilakamarri, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
SSIEM Award. Aspartoacylase deficiency: the enzyme defect in Canavan diseaseR Matalon, R Kaul, J Casanova, et al.
Pageof 19

Showing results (111-120 of 185) with videos related to

Sort By:
Pageof 19
Nephron|January 1, 1974
Hemodialysis using femoral vessel cannulationB D Nidus, R Matalon, L A Katz, et al.
American Journal of Human Genetics|July 1, 1994
Canavan disease: mutations among Jewish and non-Jewish patientsR Kaul, G P Gao, M Aloya, et al.
The Journal of Infectious Diseases|December 1, 1971
The use of gentamicin in peritoneal dialysis. II. Microbiologic and clinical resultsP J Hyams, T Smithivas, R Matalon, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Malonic aciduria and cardiomyopathyR Matalon, K Michaels, R Kaul, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1996
Gene therapy for metachromatic leukodystrophyT Ohashi, K Watabe, Y Sato, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Frequency of 12 mutations in 114 children with phenylketonuria in the Midwest region of the USAR Kaul, R Matalon, R Allen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1990
Ocular histopathology and ultrastructure of Morquio syndrome (systemic mucopolysaccharidosis IV A)M Iwamoto, Y Nawa, I H Maumenee, et al.
European Journal of Pediatrics|July 1, 1996
Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994R Koch, H Levy, W Hanley, et al.
Molecular Genetics and Metabolism Reports|October 20, 2025
Carbonic anhydrase VA deficiency due to a novel <i>CA5A</i> variantLaura Keehan, Elizabeth Null, Lekha Chilakamarri, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
SSIEM Award. Aspartoacylase deficiency: the enzyme defect in Canavan diseaseR Matalon, R Kaul, J Casanova, et al.
Pageof 19