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P M Mathew

Showing results (11-20 of 25) with videos related to

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Clinical Pediatrics|May 1, 1988
Neonatal diabetes mellitus in first cousinsP M Mathew, R W Hann, J A Hamdan
Archives of Disease in Childhood|October 1, 1989
Complications of diazoxide treatment in persistent neonatal hyperinsulinismY K Abu-Osba, K B Manasra, P M Mathew
Annals of Tropical Paediatrics|September 1, 1986
Hypoparathyroidism in Arab childrenP M Mathew, J A Hamdan, A Mallouh, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|October 1, 1971
Psychosomatic aspects of rehabilitation of leprosy patientsA Verghese, P M Mathew, L A Senseman, et al.
American Journal of Human Genetics|February 1, 1995
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, D M Hallman, et al.
Annals of Tropical Paediatrics|January 1, 1994
Familial nesidioblastosis: more evidence for autosomal recessive inheritanceM P Cherian, M J Haddad, A R Sa'di, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 20, 2001
Rickets as an unusual initial presentation of abetalipoproteinemia and hypobetalipoproteinemiaH Narchi, S S Amr, P M Mathew, et al.
Postgraduate Medical Journal|October 1, 1983
Ethnic differences in the distribution of congenital malformationsP B Terry, P M Mathew, R G Condie, et al.
Archives of Disease in Childhood|September 1, 1985
Ethnic differences in congenital malformationsP B Terry, J G Bissenden, R G Condie, et al.
Proceedings of the Association of American Physicians|January 1, 1996
The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Clinical Pediatrics|May 1, 1988
Neonatal diabetes mellitus in first cousinsP M Mathew, R W Hann, J A Hamdan
Archives of Disease in Childhood|October 1, 1989
Complications of diazoxide treatment in persistent neonatal hyperinsulinismY K Abu-Osba, K B Manasra, P M Mathew
Annals of Tropical Paediatrics|September 1, 1986
Hypoparathyroidism in Arab childrenP M Mathew, J A Hamdan, A Mallouh, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|October 1, 1971
Psychosomatic aspects of rehabilitation of leprosy patientsA Verghese, P M Mathew, L A Senseman, et al.
American Journal of Human Genetics|February 1, 1995
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, D M Hallman, et al.
Annals of Tropical Paediatrics|January 1, 1994
Familial nesidioblastosis: more evidence for autosomal recessive inheritanceM P Cherian, M J Haddad, A R Sa'di, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 20, 2001
Rickets as an unusual initial presentation of abetalipoproteinemia and hypobetalipoproteinemiaH Narchi, S S Amr, P M Mathew, et al.
Postgraduate Medical Journal|October 1, 1983
Ethnic differences in the distribution of congenital malformationsP B Terry, P M Mathew, R G Condie, et al.
Archives of Disease in Childhood|September 1, 1985
Ethnic differences in congenital malformationsP B Terry, J G Bissenden, R G Condie, et al.
Proceedings of the Association of American Physicians|January 1, 1996
The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Pageof 3