A Case with Laron Syndrome by İlker Tolga ÖZGEN, Esra KUTLU, Yaşar CESUR, Gözde YEŞİL

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Laron syndrome: An experience of treatment of two cases by Hiya Boro, Sk Hammadur Rahman, Saurav Khatiwada, Sarah Alam, Rajesh Khadgawat

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A CLINICAL CASE OF LARON SYNDROME IN THREE SIBLINGS by Яна Вячеславовна Юнкина, Алла Дмитриевна Алексеева, Галина Андреевна Поленчик, Наталья Александровна Жданова

“…This article describes a case of Laron syndrome in three children from the same family.…”
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Laron syndrome: clinic, diagnostics (а clinical case) by P.M. Lіashuk, R.P. Lіashuk, N.I. Stankova, M.B. Kudina

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Clinical features and endocrine profile of Laron syndrome in Indian children by Supriya R Phanse-Gupte, Vaman V Khadilkar, Anuradha V Khadilkar

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Marjolin’s Ulcer in Laron Syndrome - an Unexpected Combination: A Case Report by de la Paz EM

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Laron Syndrome Research Paves the Way for New Insights in Oncological Investigation by Haim Werner, Rive Sarfstein, Karthik Nagaraj, Zvi Laron

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Insulin-like growth factors and aging: lessons from Laron syndrome by Haim Werner, Zvi Laron

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Genome-Wide Profiling of Laron Syndrome Patients Identifies Novel Cancer Protection Pathways by Haim Werner, Lena Lapkina-Gendler, Laris Achlaug, Karthik Nagaraj, Lina Somri, Danielle Yaron-Saminsky, Metsada Pasmanik-Chor, Rive Sarfstein, Zvi Laron, Shoshana Yakar

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Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report by Corneli Ginevra, Aimaretti Gianluca, Curtò Lorenzo, Santarpia Libero, Cotta Oana R, Trimarchi Francesco, Cannavò Salvatore

“…<p>Abstract</p> <p>Introduction</p> <p>Primary growth hormone resistance or growth hormone insensitivity syndrome, also known as Laron syndrome, is a hereditary disease caused by deletions or different types of mutations in the growth hormone receptor gene or by post-receptor defects. …”
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Effects of GHR Deficiency and Juvenile Hypoglycemia on Immune Cells of a Porcine Model for Laron Syndrome by Marie-Christin Schilloks, Isabella-Maria Giese, Arne Hinrichs, Lucia Korbonits, Stefanie M. Hauck, Eckhard Wolf, Cornelia A. Deeg

Subjects: “…Laron syndrome…”
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Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome by Ran Li, Fengying Gong, Hui Pan, Hanting Liang, Hui Miao, Yuxing Zhao, Lian Duan, Hongbo Yang, Linjie Wang, Shi Chen, Huijuan Zhu

Subjects: “…Laron syndrome…”
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MicroRNA 132-3p Is Upregulated in Laron Syndrome Patients and Controls Longevity Gene Expression by Danielle Yaron-Saminsky, Karthik Nagaraj, Rive Sarfstein, Zvi Laron, Metsada Pasmanik-Chor, Haim Werner

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Role of the GH-IGF1 axis on the hypothalamus–pituitary–testicular axis function: lessons from Laron syndrome by Rossella Cannarella, Andrea Crafa, Sandro La Vignera, Rosita A Condorelli, Aldo E Calogero

Subjects: “…laron syndrome…”
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Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: a case report by Stefania Moia, Daniele Tessaris, Silvia Einaudi, Luisa de Sanctis, Gianni Bona, Simonetta Bellone, Flavia Prodam

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Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver by Arne Hinrichs, Barbara Kessler, Mayuko Kurome, Andreas Blutke, Elisabeth Kemter, Maren Bernau, Armin M. Scholz, Birgit Rathkolb, Simone Renner, Sebastian Bultmann, Heinrich Leonhardt, Martin Hrabĕ de Angelis, Hiroshi Nagashima, Andreas Hoeflich, Werner F. Blum, Martin Bidlingmaier, Rüdiger Wanke, Maik Dahlhoff, Eckhard Wolf

“…Objective: Laron syndrome (LS) is a rare, autosomal recessive disorder in humans caused by loss-of-function mutations of the growth hormone receptor (GHR) gene. …”
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Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report by Fatemeh Bitarafan, Mehrnoosh Khodaeian, Fatemeh Garrousi, Raziyeh Khalesi, Donya Ghazi Nader, Behnam Karimi, Reza Alibakhshi, Masoud Garshasbi

Subjects: “…Laron Syndrome (LS)…”
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Over-stimulation of insulin/IGF-1 signaling by western diet may promote diseases of civilization: <it>lessons learnt from laron syndrome</it> by Schmitz Gerd, John Swen, Melnik Bodo C

“…Individuals with Laron syndrome who carry mutations in the growth hormone receptor (<it>GHR</it>) gene that lead to severe congenital IGF-1 deficiency with decreased insulin/IGF-1 signaling (IIS) exhibit reduced prevalence rates of acne, diabetes and cancer. …”
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Generation of GHR-modified pigs as Laron syndrome models via a dual-sgRNAs/Cas9 system and somatic cell nuclear transfer by Honghao Yu, Weihu Long, Xuezeng Zhang, Kaixiang Xu, Jianxiong Guo, Heng Zhao, Honghui Li, Yubo Qing, Weirong Pan, Baoyu Jia, Hong-Ye Zhao, Xingxu Huang, Hong-Jiang Wei

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Growth hormone insensitivity syndrome: A sensitive approach by Soumik Goswami, Sujoy Ghosh, Subhankar Chowdhury

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