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M Guftar Shaikh

Showing results (11-20 of 31) with videos related to

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Archives of Disease in Childhood|March 27, 2016
Permanent congenital hypothyroidism with blood spot thyroid stimulating hormone <10 mU/LJeremy H Jones, Sarah Smith, Catherine Dorrian, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 11, 2006
Thyroxine: cause and cure for headacheM Guftar Shaikh, Nalin Wickramasuriya, Karen McLachlan, et al.
European Journal of Pediatrics|April 15, 2021
An appraisal of current service delivery and future models of care for young people with gender dysphoriaStephanie McCallion, Simon Smith, Heather Kyle, et al.
Archives of Disease in Childhood|March 12, 2016
How well does the capillary thyroid-stimulating hormone test for newborn thyroid screening predict the venous free thyroxine level?Tzveta Pokrovska, Jeremy Jones, M Guftar Shaikh, et al.
Hormone Research in Paediatrics|November 1, 2014
Longitudinal changes in body mass index in children with craniopharyngiomaMuhammad Jaffar Khan, Khadija Nuzhat Humayun, Malcolm Donaldson, et al.
Clinical Endocrinology|December 9, 2020
The use of growth hormone therapy in adults with Prader-Willi syndrome: A systematic reviewMikaela Frixou, Diane Vlek, Angela K Lucas-Herald, et al.
Microbiome|July 2, 2024
CViewer: a Java-based statistical framework for integration of shotgun metagenomics with other omics datasetsOrges Koci, Richard K Russell, M Guftar Shaikh, et al.
International Journal of Pediatric Endocrinology|April 17, 2015
The pitfalls associated with urinary steroid metabolite ratios in children undergoing investigations for suspected disorders of steroid synthesisAngela K Lucas-Herald, Martina Rodie, Laura Lucaccioni, et al.
Hormone Research in Paediatrics|July 19, 2018
Single-Centre Experience of Testosterone Therapy for Boys with HypogonadismAngela K Lucas-Herald, Eliot Mason, Paula Beaumont, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 20, 2018
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of LifeFiliz Mine Çizmecioğlu, Jeremy Huw Jones, Wendy Forsyth Paterson, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Archives of Disease in Childhood|March 27, 2016
Permanent congenital hypothyroidism with blood spot thyroid stimulating hormone <10 mU/LJeremy H Jones, Sarah Smith, Catherine Dorrian, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 11, 2006
Thyroxine: cause and cure for headacheM Guftar Shaikh, Nalin Wickramasuriya, Karen McLachlan, et al.
European Journal of Pediatrics|April 15, 2021
An appraisal of current service delivery and future models of care for young people with gender dysphoriaStephanie McCallion, Simon Smith, Heather Kyle, et al.
Archives of Disease in Childhood|March 12, 2016
How well does the capillary thyroid-stimulating hormone test for newborn thyroid screening predict the venous free thyroxine level?Tzveta Pokrovska, Jeremy Jones, M Guftar Shaikh, et al.
Hormone Research in Paediatrics|November 1, 2014
Longitudinal changes in body mass index in children with craniopharyngiomaMuhammad Jaffar Khan, Khadija Nuzhat Humayun, Malcolm Donaldson, et al.
Clinical Endocrinology|December 9, 2020
The use of growth hormone therapy in adults with Prader-Willi syndrome: A systematic reviewMikaela Frixou, Diane Vlek, Angela K Lucas-Herald, et al.
Microbiome|July 2, 2024
CViewer: a Java-based statistical framework for integration of shotgun metagenomics with other omics datasetsOrges Koci, Richard K Russell, M Guftar Shaikh, et al.
International Journal of Pediatric Endocrinology|April 17, 2015
The pitfalls associated with urinary steroid metabolite ratios in children undergoing investigations for suspected disorders of steroid synthesisAngela K Lucas-Herald, Martina Rodie, Laura Lucaccioni, et al.
Hormone Research in Paediatrics|July 19, 2018
Single-Centre Experience of Testosterone Therapy for Boys with HypogonadismAngela K Lucas-Herald, Eliot Mason, Paula Beaumont, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 20, 2018
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of LifeFiliz Mine Çizmecioğlu, Jeremy Huw Jones, Wendy Forsyth Paterson, et al.
Pageof 4