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The Journal of Antimicrobial Chemotherapy
|
April 1, 1994
Treatment of candiduria with liposomal amphotericin B (L-AmpB-LRC) in children
P C Gokhale, N A Kshirsagar, M U Khan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
September 1, 2004
A nonsense mutation (E72X) in growth hormone releasing hormone receptor (GHRHR) gene is the major cause of familial isolated growth hormone deficiency in Western region of India: founder effect suggested by analysis of dinucleotide repeat polymorphism close to GHRHR gene
Takashi Kamijo, Yoshitaka Hayashi, Hisao Seo, et al.
Indian Pediatrics
|
November 1, 1982
Therapy of childhood hypothyroidism: a reappraisal
M Desai, A J Irani, M P Colaco, et al.
Indian Pediatrics
|
January 1, 1983
Thyroid hormones and TSH in normal children and hypothyroids
M Desai, A J Irani, M P Colaco, et al.
Indian Journal of Pediatrics
|
July 1, 1987
Neonatal screening for congenital hypothyroidism in a developing country: problems and strategies
M P Desai, M P Colaco, A R Ajgaonkar, et al.
Hemoglobin
|
January 11, 2019
Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India
Ajit C Gorakshakar, Pearl V Breganza, Stacy P Colaco, et al.
Indian Pediatrics
|
September 1, 1984
Neonatal screening for hypothyroidism
M P Colaco, M P Desai, A R Ajgaonkar, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
The Journal of Antimicrobial Chemotherapy
|
April 1, 1994
Treatment of candiduria with liposomal amphotericin B (L-AmpB-LRC) in children
P C Gokhale, N A Kshirsagar, M U Khan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
September 1, 2004
A nonsense mutation (E72X) in growth hormone releasing hormone receptor (GHRHR) gene is the major cause of familial isolated growth hormone deficiency in Western region of India: founder effect suggested by analysis of dinucleotide repeat polymorphism close to GHRHR gene
Takashi Kamijo, Yoshitaka Hayashi, Hisao Seo, et al.
Indian Pediatrics
|
November 1, 1982
Therapy of childhood hypothyroidism: a reappraisal
M Desai, A J Irani, M P Colaco, et al.
Indian Pediatrics
|
January 1, 1983
Thyroid hormones and TSH in normal children and hypothyroids
M Desai, A J Irani, M P Colaco, et al.
Indian Journal of Pediatrics
|
July 1, 1987
Neonatal screening for congenital hypothyroidism in a developing country: problems and strategies
M P Desai, M P Colaco, A R Ajgaonkar, et al.
Hemoglobin
|
January 11, 2019
Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India
Ajit C Gorakshakar, Pearl V Breganza, Stacy P Colaco, et al.
Indian Pediatrics
|
September 1, 1984
Neonatal screening for hypothyroidism
M P Colaco, M P Desai, A R Ajgaonkar, et al.
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of 3