Recent Publications on Laron Syndrome: |  |
| Growth hormone responsiveness: peak stimulated growth hormone levels and other variables in idiopathic short stature (ISS): data from the National Cooperative Growth Study.
| 23rd September, 2008
| Pediatric Endocrinology, Children's Mercy Hospital/University of
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Mecasermin rinfabate: rhIGF-I/rhIGFBP-3 complex: iPLEX.
BACKGROUND: Mecasermin rinfabate (iPLEX), comprising rhIGF-I complexed to...
Direct Link | 13th August, 2008
| University of Cambridge, Department of Paediatrics, Addenbrookes Hospital,
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| Statement 6: patients who are unresponsive to GH therapy should be given a trial of IGF-I.
| 29th July, 2008
| Division of Endocrinology, Metabolism & Diabetes, Department of
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| Statement 5: the first line of treatment for children with idiopathic short stature (ISS) and low serum insulin-like growth factor-I (IGF-I) should be IGF-I.
| 29th July, 2008
| Department of Pediatrics, Cincinnati Children's Hospital Medical Center,
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| Statement 3: a low serum IGF-I Level in idiopathic short stature patients indicates partial GH insensitivity.
| 29th July, 2008
| Pediatric Endocrinology Unit, Karolinska Institute & University Hospital
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| Insulin-like growth factor-I treatment of children with Laron syndrome (primary growth hormone insensitivity).
| 17th May, 2008
| Endocrinology and Diabetes Research Unit, Schneider Children's Medical
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| Foot length before and during insulin-like growth factor-I treatment of children with laron syndrome compared to human growth hormone treatment of children with isolated growth hormone deficiency.
| 13th May, 2008
| Endocrinology and Diabetes Research Unit, Schneider Children's Medical
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Nonalcoholic fatty liver in patients with Laron syndrome and GH gene deletion - preliminary report.
BACKGROUND: There is little information on the relationship between growth...
Direct Link | 9th May, 2008
| Endocrinology and Diabetes Research Unit, Schneider Children's Medical
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| Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism.
| 1st May, 2008
| Faculty of Engineering, Marmara University, Istanbul.
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[New molecular mechanisms of growth hormone insensitivity]
Growth hormone (GH), secreted by the anterior pituitary into the...
Direct Link | 29th April, 2008
| Service d'endocrinologie pediatrique, hopital des enfants, place du
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| The GH-IGF1 axis and longevity. The paradigm of IGF1 deficiency.
| 24th April, 2008
| Endocrinology and Diabetes Research Unit, Schneider Children's Medical
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Growth hormone (GH) insensitivity and insulin-like growth factor-I deficiency in Inuit subjects and an Ecuadorian cohort: functional studies of two codon 180 GH receptor gene mutations.
CONTEXT: Among more than 250 cases of GH insensitivity syndrome (GHIS)...
Direct Link | 16th April, 2008
| Department of Pediatrics, NRC5, Oregon Health and Science University, 3181
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| Lessons from the genetics of laron syndrome.
| 15th April, 2008
| Department of Pediatrics, University of Florida College of Medicine,
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Serum ghrelin concentrations are increased in children with growth hormone insensitivity and decrease during long-term insulinlike growth factor-I treatment.
BACKGROUND: Ghrelin increases food intake, body weight, and growth hormone...
Direct Link | 26th March, 2008
| Department of Pediatrics, Division of Endocrinology, The University of
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