Endocrine Abstracts Search

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Showing page 1 of results 1 - 10 of about 102 matches for "senniappan-senthil"

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Hypoglycaemic disorders in Neonates & Children
Senthil Senniappan
http://www.endocrine-abstracts.org/ea/0051/ea0051cme2.htm
Published: 2017-10-30

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Hyperinsulinism Hyperammonemia (HI/HA) syndrome due to GLUD1 mutation: Phenotypic Variations Ranging from Late Presentation to Spontaneous Resolution
Agnieszka Brandt; Dinesh Giri; Zoe Yung; Mohammad Didi; Senthil Senniappan
http://www.endocrine-abstracts.org/ea/0051/ea0051p064.htm
Published: 2017-10-30

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Novel splicing mutation in B3GAT3 associated with short stature, GH deficiency, hypoglycaemia, developmental delay and multiple congenital anomalies
Samuel Bloor; Dinesh Giri; Mohammed Didi; Senthil Senniappan
http://www.endocrine-abstracts.org/ea/0051/ea0051p021.htm
Published: 2017-10-30

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Calcium/calmodulin dependent protein kinase 2 (CaMKK2) mutation a novel genetic cause of congenital hyperinsulinism
Dinesh Giri; John Scott; Bruce Kemp; Mohammed Didi; Anthony Means; Senthil Senniappan
http://www.endocrine-abstracts.org/ea/0051/ea0051p019.htm
Published: 2017-10-30

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Follicular thyroid carcinoma due to a heterozygous gain of function mutation in thyrotropin receptor (TSHR)
James Blackburn; Dinesh Giri; Senthil Seniappan; Mohammed Didi; Barbara Ciolka; Matthew Jones; George Kokai; Alison Waghorn; Nic
http://www.endocrine-abstracts.org/ea/0051/ea0051p005.htm
Published: 2017-10-30

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Long-term follow-up of Graves disease in Adolescents: a 10 year study from a single UK tertiary centre
Judy Li; Dinesh Giri; Renuka Ramakrishnan; Urmi Das; Poonam Dharmaraj; Jo Blair; Mohammad Didi; Senthil Senniappan
http://www.endocrine-abstracts.org/ea/0051/ea0051p003.htm
Published: 2017-10-30

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Assessment of adrenal function and recovery of HPA axis in children with chronic asthma assessed by LDSST
Arundoss Gangadharan; Mohammed Didi; Urmi Das; Poonam Dharmaraj; Senthil Senniappan; Renuka Ramakrishnan; Jo Blair
http://www.endocrine-abstracts.org/ea/0051/ea0051oc8.2.htm
Published: 2017-10-30

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Novel FOXA2 mutation causes hyperinsulinism, hypopituitarism with craniofacial dysmorphism and endoderm-derived organ abnormalities
Dinesh Giri; Marial Lillina Vignola; Angelica Gualtieri; Valeria Scagliotti; Paul McNamara; Matthew Peak; Mohammed Didi; Carles
http://www.endocrine-abstracts.org/ea/0051/ea0051oc4.3.htm
Published: 2017-10-30

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Testosterone Therapy Improves the First Year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty
Dinesh Giri; Prashant Patil; Jo Blair; Urmi Das; Renuka Ramakrishnan; Poonam Dharmaraj; Mohammed Didi; Senthil Senniappan
http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p840.htm
Published: 2016-08-19

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A Study of Bone Health Index (BHI) in Girls with Turners Syndrome
Carley Frerichs; Carly Jenkinson; Anne Povall; Laurence Abernethy; Urmi Das; Renuka Ramakrishnan; Senthil Senniappan; Mohammed D
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p828.htm
Published: 2016-08-19