Congenital Leptin Deficiency Due to Homozygosity for the Δ133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy
Gibson, William T, Farooqi, I. Sadaf, Moreau, Mary, DePaoli, Alex M, Lawrence, Elizabeth, O’Rahilly, Stephen, Trussell, Rebecca A
Published in The journal of clinical endocrinology and metabolism (01.10.2004)
Published in The journal of clinical endocrinology and metabolism (01.10.2004)
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Journal Article
Development of a simple tool for diagnosis and initial approach to hypertension and pre-hypertension in children and youth
Grisaru, Silviu, Watson-Jarvis, Kay, McKenna, Catherine M., Ho, Josephine, Harder, Joyce R., Trussell, Rebecca A.
Published in Open journal of pediatrics (2012)
Published in Open journal of pediatrics (2012)
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Journal Article
Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy
Gibson, William T, Farooqi, I Sadaf, Moreau, Mary, DePaoli, Alex M, Lawrence, Elizabeth, O'Rahilly, Stephen, Trussell, Rebecca A
Published in The journal of clinical endocrinology and metabolism (01.10.2004)
Get full text
Published in The journal of clinical endocrinology and metabolism (01.10.2004)
Journal Article
Congenital leptin deficiency due to homozygosity for the A133G mutation: Report of another case and evaluation of response to four years of leptin therapy
GIBSON, William T, SADAF FAROOQI, I, MOREAU, Mary, DEPAOLI, Alex M, LAWRENCE, Elizabeth, O'RAHILLY, Stephen, TRUSSELL, Rebecca A
Published in The journal of clinical endocrinology and metabolism (2004)
Get full text
Published in The journal of clinical endocrinology and metabolism (2004)
Journal Article