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Safety and effectiveness of taliglucerase alfa in patients with Gaucher disease: an interim analysis of real-world data from a multinational drug registry (TALIAS)

Orphanet journal of rare diseases, 2022-04, Vol.17 (1), p.145-145, Article 145

2022

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Persistence with daily growth hormone among children and adolescents with growth hormone deficiency in the UK

Frontiers in endocrinology (Lausanne), 2022-11, Vol.13, p.1014743-1014743

2022

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An overview of growth hormone therapy in pediatric cases documented in the Kabi International Growth Study (Pfizer International Growth Database)

Annals of pediatric endocrinology & metabolism, 2024-02, Vol.29 (1), p.3-11

2024

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Gender of Pediatric Recombinant Human Growth Hormone Recipients in the United States and Globally

The journal of clinical endocrinology and metabolism, 2008-06, Vol.93 (6), p.2050-2056

2008

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More than a decade of real-world experience of pegvisomant for acromegaly: ACROSTUDY

European journal of endocrinology, 2021-10, Vol.185 (4), p.525

2021

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Limited Efficacy of Growth Hormone (GH) during Transition of GH-Deficient Patients from Adolescence to Adulthood: A Phase III Multicenter, Double-Blind, Randomized Two-Year Trial

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.3946-3955

2005

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Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study

The journal of clinical endocrinology and metabolism, 2022-06, Vol.107 (7), p.e2717-e2728

2022

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Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

The journal of clinical endocrinology and metabolism, 2022-11, Vol.107 (12), p.3287-3301

2022

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Suboptimal adherence to daily growth hormone in a US real-world study: an unmet need in the treatment of pediatric growth hormone deficiency

Current medical research and opinion, 2021-12, Vol.37 (12), p.2141-2150

2021

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Long-term safety of growth hormone in adults with growth hormone deficiency: Overview of 15,809 GH-treated patients

The journal of clinical endocrinology and metabolism, 2022-07, Vol.107 (7), p.1906-1919

2022

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A Randomized, Cross‐Over Study Investigating the Comparability of Somatrogon‐ghla in 2 Different Drug Product Presentations

Clinical pharmacology in drug development, 2024-06

2024

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Patient-reported outcomes in patients with acromegaly treated with pegvisomant in the ACROSTUDY extension: A real-world experience

Pituitary, 2022-06, Vol.25 (3), p.420-432

2022

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A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness

The journal of clinical endocrinology and metabolism, 2020-10, Vol.105 (10), p.3203-3214

2020

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Response to Letter to the Editor: “A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness”

The journal of clinical endocrinology and metabolism, 2021-01, Vol.106 (1), p.e409-e410

2021

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Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little ( lit ) mouse

Nature genetics, 1996-01, Vol.12 (1), p.88-90

1996

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Suboptimal adherence to prescribed daily growth hormone regimen among medicaid beneficiaries in the United States

Current medical research and opinion, 2022-06, Vol.38 (6), p.917-925

2022

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Growth Hormone Releasing Hormone (GHRH) and the GHRH Receptor

Reviews in endocrine & metabolic disorders, 2002-12, Vol.3 (4), p.313-323

2002

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Response to Letter to the Editor From Virú-Loza and Chávez-Nomberto: “Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort”

The journal of clinical endocrinology and metabolism, 2023-06, Vol.108 (6), p.e356-e357

2023

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Ease of use and preference for a new disposable self-injection pen compared with a reusable pen for administering recombinant human growth hormone: A multicenter, 2-Month, single-arm, open-label clinical trial in patient-caregiver dyads

Clinical therapeutics, 2010-11, Vol.32 (12), p.2036-2047

2010

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Treatment of Acromegaly with Pegvisomant during Pregnancy: Maternal and Fetal Effects

The journal of clinical endocrinology and metabolism, 2007-09, Vol.92 (9), p.3374-3377

2007

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Efficacy of growth hormone therapy in Kearns-Sayre syndrome: the KIGS experience

Journal of pediatric endocrinology & metabolism : JPEM, 2016-11, Vol.29 (11), p.1319

2016

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A longer interval without GH replacement and female gender are associated with lower bone mineral density in adults with childhood-onset GH deficiency: a KIMS database analysis

European journal of endocrinology, 2012-09, Vol.167 (3), p.343

2012

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Response to Growth hormone deficiency in mitochondrial disorders

Journal of pediatric endocrinology & metabolism : JPEM, 2017-04, Vol.30 (4), p.483

2017

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Unreplaced Sex Steroid Deficiency, Corticotropin Deficiency, and Lower IGF-I Are Associated with Lower Bone Mineral Density in Adults with Growth Hormone Deficiency: A KIMS Database Analysis

The journal of clinical endocrinology and metabolism, 2011-05, Vol.96 (5), p.1516-1523

2011

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Variable Phenotypes in Familial Isolated Growth Hormone Deficiency Caused by a G6664A Mutation in the GH-1 Gene

The journal of clinical endocrinology and metabolism, 2007-11, Vol.92 (11), p.4387-4393

2007

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Safety and effectiveness of taliglucerase alfa in patients with Gaucher disease: an interim analysis of real-world data from a multinational drug registry (TALIAS)

Persistence with daily growth hormone among children and adolescents with growth hormone deficiency in the UK

An overview of growth hormone therapy in pediatric cases documented in the Kabi International Growth Study (Pfizer International Growth Database)

Gender of Pediatric Recombinant Human Growth Hormone Recipients in the United States and Globally

More than a decade of real-world experience of pegvisomant for acromegaly: ACROSTUDY

Limited Efficacy of Growth Hormone (GH) during Transition of GH-Deficient Patients from Adolescence to Adulthood: A Phase III Multicenter, Double-Blind, Randomized Two-Year Trial

Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study

Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

Suboptimal adherence to daily growth hormone in a US real-world study: an unmet need in the treatment of pediatric growth hormone deficiency

Long-term safety of growth hormone in adults with growth hormone deficiency: Overview of 15,809 GH-treated patients

A Randomized, Cross‐Over Study Investigating the Comparability of Somatrogon‐ghla in 2 Different Drug Product Presentations

Patient-reported outcomes in patients with acromegaly treated with pegvisomant in the ACROSTUDY extension: A real-world experience

A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness

Response to Letter to the Editor: “A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness”

Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little ( lit ) mouse

Suboptimal adherence to prescribed daily growth hormone regimen among medicaid beneficiaries in the United States

Growth Hormone Releasing Hormone (GHRH) and the GHRH Receptor

Response to Letter to the Editor From Virú-Loza and Chávez-Nomberto: “Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort”

Ease of use and preference for a new disposable self-injection pen compared with a reusable pen for administering recombinant human growth hormone: A multicenter, 2-Month, single-arm, open-label clinical trial in patient-caregiver dyads

Treatment of Acromegaly with Pegvisomant during Pregnancy: Maternal and Fetal Effects

Efficacy of growth hormone therapy in Kearns-Sayre syndrome: the KIGS experience

A longer interval without GH replacement and female gender are associated with lower bone mineral density in adults with childhood-onset GH deficiency: a KIMS database analysis

Response to Growth hormone deficiency in mitochondrial disorders

Unreplaced Sex Steroid Deficiency, Corticotropin Deficiency, and Lower IGF-I Are Associated with Lower Bone Mineral Density in Adults with Growth Hormone Deficiency: A KIMS Database Analysis

Variable Phenotypes in Familial Isolated Growth Hormone Deficiency Caused by a G6664A Mutation in the GH-1 Gene

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