[Growth hormone deficiency in children. Diagnostic methods]

Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating Investigators.

The Journal of pediatrics·1998

Long-term results of growth hormone treatment in France in children of short stature: population, register based study.

BMJ (Clinical research ed.)·1997

Growth hormone testing for the diagnosis of growth hormone deficiency in childhood: a population register-based study.

The Journal of clinical endocrinology and metabolism·1997

Follow-up of three years of treatment with growth hormone and of one post-treatment year, in children with severe growth retardation of intrauterine onset.

Pediatric research·1996

Growth and puberty in a fostered kindred.

European journal of pediatrics·1994

Dose-dependent catch-up growth after 2 years of growth hormone treatment in intrauterine growth-retarded children. Belgian and French Pediatric Clinics and Sanofi-Choay (France).

The Journal of clinical endocrinology and metabolism·1994

[Advances and perspectives in vascularized composite allotransplantation preservation].

Bulletin de l'Academie nationale de medecine·2025

[COVID-19: Neurological manifestations and complications during the acute phase of the disease].

Bulletin de l'Academie nationale de medecine·2024

[Role of psychological factors in post-COVID-19 condition].

Bulletin de l'Academie nationale de medecine·2023

[Neurological forms of long COVID in adults: Critical approach].

Bulletin de l'Academie nationale de medecine·2023

[Post-COVID-19 syndrome].

Bulletin de l'Academie nationale de medecine·2023

The next psychoactive drugs: From imipramine to ketamine.

Bulletin de l'Academie nationale de medecine·2023

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Cureus·2026

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Molecular syndromology·2026

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

Journal of immunology (Baltimore, Md. : 1950)·2026

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Arquivos de neuro-psiquiatria·2026

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

Gene·2026

Developmental Profiles Associated with TUBA1A, TUBB2A, TUBB2B, and TUBB3 Tubulinopathy Conditions.

American journal on intellectual and developmental disabilities·2026

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[Growth hormone deficiency in children. Diagnostic methods]

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Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating Investigators.

Long-term results of growth hormone treatment in France in children of short stature: population, register based study.

Growth hormone testing for the diagnosis of growth hormone deficiency in childhood: a population register-based study.

Follow-up of three years of treatment with growth hormone and of one post-treatment year, in children with severe growth retardation of intrauterine onset.

Growth and puberty in a fostered kindred.

Dose-dependent catch-up growth after 2 years of growth hormone treatment in intrauterine growth-retarded children. Belgian and French Pediatric Clinics and Sanofi-Choay (France).

[Advances and perspectives in vascularized composite allotransplantation preservation].

[COVID-19: Neurological manifestations and complications during the acute phase of the disease].

[Role of psychological factors in post-COVID-19 condition].

[Neurological forms of long COVID in adults: Critical approach].

[Post-COVID-19 syndrome].

The next psychoactive drugs: From imipramine to ketamine.

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

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[Growth hormone deficiency in children. Diagnostic methods]

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