[Hypothyroidism in child]

Same author

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

Orphanet journal of rare diseases·2026

Same author

APPROACH TO THE PATIENT: Genetics and Management of Congenital Hypothyroidism.

The Journal of clinical endocrinology and metabolism·2026

Same author

Rare Causes of Pediatric Primary Adrenal Insufficiency: An Observational Cohort Study.

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists·2026

Same author

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

Annales d'endocrinologie·2026

Same author

Letter to the editor from Miller et al: "long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index".

The Journal of clinical endocrinology and metabolism·2026

Same author

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

Annales d'endocrinologie·2026

Same journal

[Prolonged fever].

La Revue du praticien·2026

Same journal

[Lower gastrointestinal bleeding].

La Revue du praticien·2026

Same journal

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

La Revue du praticien·2026

Same journal

[A history of child abuse intervention in the West].

La Revue du praticien·2026

Same journal

[Agranulocytose médicamenteuse].

La Revue du praticien·2026

Same journal

[Patient education in heart failure].

La Revue du praticien·2026

Related Experiment Videos

[Hypothyroidism in child]

Related Concept Videos

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

APPROACH TO THE PATIENT: Genetics and Management of Congenital Hypothyroidism.

Rare Causes of Pediatric Primary Adrenal Insufficiency: An Observational Cohort Study.

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

Letter to the editor from Miller et al: "long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index".

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

[Prolonged fever].

[Lower gastrointestinal bleeding].

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

[A history of child abuse intervention in the West].

[Agranulocytose médicamenteuse].

[Patient education in heart failure].

Related Experiment Videos

[Hypothyroidism in child]

Related Concept Videos

Related Articles

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

APPROACH TO THE PATIENT: Genetics and Management of Congenital Hypothyroidism.

Rare Causes of Pediatric Primary Adrenal Insufficiency: An Observational Cohort Study.

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

Letter to the editor from Miller et al: "long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index".

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.

[Prolonged fever].

[Lower gastrointestinal bleeding].

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

[A history of child abuse intervention in the West].

[Agranulocytose médicamenteuse].

[Patient education in heart failure].