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R Lala

Showing results (71-80 of 79) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 26, 1999
A novel GNAS1 mutation, R201G, in McCune-albright syndromeM Riminucci, L W Fisher, A Majolagbe, et al.
Clinical Endocrinology|June 1, 1990
Arginine potentiates the GHRH- but not the pyridostigmine-induced GH secretion in normal short children. Further evidence for a somatostatin suppressing effect of arginineE Ghigo, J Bellone, E Mazza, et al.
Hormone Research in Paediatrics|September 26, 2012
Thyroid abnormalities in children and adolescents with McCune-Albright syndromeD Tessaris, A Corrias, P Matarazzo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 28, 2011
Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disordersA Mussa, F Porta, G Baldassarre, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 26, 2010
Laparoscopic unilateral adrenalectomy in children for isolated primary pigmented nodular adrenocortical disease (PPNAD): case report and literature reviewR Guanà, R Gesmundo, M Morino, et al.
Journal of Clinical Pathology|March 29, 2006
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white familyM F Campagnoli, A Pucci, E Garelli, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[Neonatal pseudohypoaldosteronism: when a denied truth can delay a diagnosis]R Bagna, P Tonetto, R Spola, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 30, 1999
McCune-Albright syndrome: a longitudinal clinical study of 32 patientsC de Sanctis, R Lala, P Matarazzo, et al.
Nature Genetics|July 1, 1997
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeM Bamshad, R C Lin, D J Law, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 26, 1999
A novel GNAS1 mutation, R201G, in McCune-albright syndromeM Riminucci, L W Fisher, A Majolagbe, et al.
Clinical Endocrinology|June 1, 1990
Arginine potentiates the GHRH- but not the pyridostigmine-induced GH secretion in normal short children. Further evidence for a somatostatin suppressing effect of arginineE Ghigo, J Bellone, E Mazza, et al.
Hormone Research in Paediatrics|September 26, 2012
Thyroid abnormalities in children and adolescents with McCune-Albright syndromeD Tessaris, A Corrias, P Matarazzo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 28, 2011
Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disordersA Mussa, F Porta, G Baldassarre, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 26, 2010
Laparoscopic unilateral adrenalectomy in children for isolated primary pigmented nodular adrenocortical disease (PPNAD): case report and literature reviewR Guanà, R Gesmundo, M Morino, et al.
Journal of Clinical Pathology|March 29, 2006
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white familyM F Campagnoli, A Pucci, E Garelli, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[Neonatal pseudohypoaldosteronism: when a denied truth can delay a diagnosis]R Bagna, P Tonetto, R Spola, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 30, 1999
McCune-Albright syndrome: a longitudinal clinical study of 32 patientsC de Sanctis, R Lala, P Matarazzo, et al.
Nature Genetics|July 1, 1997
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeM Bamshad, R C Lin, D J Law, et al.
Pageof 8