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Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

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Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.

Human mutation·1999

[Results of national evaluation tests (primary schools) of CE2 and 6th classes of 73 students with congenital hypothyroidism screened at birth].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·1999

Two cases of Townes-Brocks syndrome with previously undescribed anomalies.

Clinical dysmorphology·1998

Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardation.

Acta paediatrica (Oslo, Norway : 1992)·1998

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

The Journal of pediatrics·1998

Adrenal Incidentaloma Revealing Unrecognized 21-Hydroxylase Deficiency: From Non-Classical to Late-Onset Classical Forms.

Annales d'endocrinologie·2026

Stroke risk in diabetic patients with concomitant cardiovascular disease the CARDIAB-Stroke study.

Annales d'endocrinologie·2026

Decision-making in primary hyperparathyroidism in older patients: surgical or conservative management?

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Rebuilding Beta-Cell Function: Advances In Replacement, Preservation And Regeneration.

Annales d'endocrinologie·2026

Screening and management of menstrual cycle disorders in women athletes by sports physicians: The HYPOFIT Study.

Annales d'endocrinologie·2026

Diabetes in deprived patients.

Annales d'endocrinologie·2026

The Role of Sex Steroids, Sex Hormone-binding Globulin and Leptin in the Development of Pubertal Gynecomastia and its Persistence into Adulthood.

Journal of clinical research in pediatric endocrinology·2026

Two distributed enhancers of Sox17 additively regulate the developmental fate of bipotential ventral pancreato-biliary progenitor cells.

Development (Cambridge, England)·2026

Dlk1-deficient mice achieve puberty despite low body weight and low levels of leptin and kisspeptin.

Journal of neuroendocrinology·2026

Amyloid precursor protein dosage normalization rescues neurogenesis and Alzheimer's Disease phenotypes associated with Down Syndrome.

Medical research archives·2026

Evidence Regarding Metachromatic Leukodystrophy Newborn Screening.

Pediatrics·2026

A descriptive study of early eyelid morphogenesis in a large-scale human embryo collection.

Cells, tissues, organs·2026

Related Experiment Videos

[Endocrine function of the testis in 125 cases of cryptorchism]

Related Concept Videos

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.

[Results of national evaluation tests (primary schools) of CE2 and 6th classes of 73 students with congenital hypothyroidism screened at birth].

Two cases of Townes-Brocks syndrome with previously undescribed anomalies.

Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardation.

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

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Screening and management of menstrual cycle disorders in women athletes by sports physicians: The HYPOFIT Study.

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The Role of Sex Steroids, Sex Hormone-binding Globulin and Leptin in the Development of Pubertal Gynecomastia and its Persistence into Adulthood.

Two distributed enhancers of Sox17 additively regulate the developmental fate of bipotential ventral pancreato-biliary progenitor cells.

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[Endocrine function of the testis in 125 cases of cryptorchism]

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