Results 161 to 170 of about 3,629,719 (185)
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Hearing in Patients with Laron Syndrome
2010Untreated or late IGF-I treated patients with Laron syndrome have auditory defects. In very early treated children hearing is normal.
Zvi Laron, Omer Zarchi, Joseph Attias
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Genetic heterogeneity in Laron syndrome
Acta Paediatrica, 1993U, Francke, M A, Berg
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Insights from the clinical phenotype of subjects with Laron syndrome in Ecuador
Reviews in Endocrine & Metabolic Disorders, 2020J. Guevara-Aguirre +7 more
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Cervical Myelomalacia in Laron Syndrome
2016Laron Syndrome (LS) is characterized by inability to respond normally to growth hormone of endogenous or exogenous origin (Laron et al.). Most growth hormone effects are mediated by insulin-like growth factor 1 (IGF-1), which is the anabolic effector hormone of the pituitary growth hormone.
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In Reference to Fanconi Anemia and Laron Syndrome
The American Journal of the Medical Sciences, 2018Benilde García-de Teresa, Sara Frias
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An unusual brain lesion in a patient with Laron Syndrome
EndocrineLiora Kornreich, Z. Laron
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Emerging treatment options for patients with Laron syndrome
Expert Opinion on Orphan Drugs, 2014Zvi Laron
exaly
IGF-I deficiency, longevity and cancer protection of patients with Laron syndrome.
Mutation research. Reviews in mutation research, 2017Z. Laron +3 more
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