[Genetic basis of familial multihormonal hypothalamo-hypophyseal dwarfism in children]

Serum tryptase level is a better predictor of systemic side effects than prostaglandin D2 metabolites during venom immunotherapy in children.

Journal of investigational allergology & clinical immunology·2011

Effectiveness of the iodine prophylaxis model adopted in Poland.

Journal of endocrinological investigation·2008

Iodine deficiency disorders incidence in neonates based on the experience with mass screening for congenital hypothyroidism in southeast Poland in the years 1985-2000.

Journal of endocrinological investigation·2003

Comparative analysis of zinc status, food products' frequency intake and food habits of 11-year-old healthy children.

Food additives and contaminants·2002

[Molecular studies in a population of children with bronchial asthma. I. Polymorphism in the promotor region of gene CD14].

Pneumonologia i alergologia polska·2001

The influence of lead and cadmium environmental pollution on anthropometric health factors in children.

Przeglad lekarski·2001

Macroprolactinoma with an atypical course.

Endokrynologia Polska·2026

Impact of the use of Extended™ Wear Infusion sets on metabolic, ultrasound, and psychological outcomes in adults with type 1 diabetes using the Medtronic MiniMed 780G: a pilot randomized controlled trial.

Endokrynologia Polska·2026

The association between abdominal muscle mass quantified by computed tomography and osteoporosis in postmenopausal women.

Endokrynologia Polska·2026

Beyond traditional biopsy: integrating liquid biopsy, molecular panels, and advanced imaging techniques in thyroid cancer management.

Endokrynologia Polska·2026

Estimating obesity phenotype features in a real-world cohort - a non-interventional pilot study using an original questionnaire.

Endokrynologia Polska·2026

Type 5 diabetes mellitus: revisiting malnutrition-related diabetes.

Endokrynologia Polska·2026

Intrafamilial phenotypic variation in four Palestinian siblings with CFAP418-related ciliopathy: a familial case series.

BMC ophthalmology·2026

Genetic variants in NEF2L2 rs35652124 and GABRB3 rs2081648 genes: association with autism spectrum disorder in Iraqi children.

Neuroscience·2026

Phenotypic spectrum of 1q21.1 copy number variants in 42 children: genotype-phenotype correlations and clinical implications.

European journal of pediatrics·2026

Estimating the Heritability of Intelligence with a Nuclear Twin Family Design.

Twin research and human genetics : the official journal of the International Society for Twin Studies·2026

Gut microbiota and the gut-brain axis in autism spectrum disorder and attention-deficit/hyperactivity disorder: A scoping review of shared and disorder-specific mechanistic pathways.

AIMS microbiology·2026

Case Report: Neonatal lethality caused by novel compound heterozygous missense variants of SLC6A9 gene.

Frontiers in pediatrics·2026

Related Experiment Videos

[Genetic basis of familial multihormonal hypothalamo-hypophyseal dwarfism in children]

Related Concept Videos

Serum tryptase level is a better predictor of systemic side effects than prostaglandin D2 metabolites during venom immunotherapy in children.

Effectiveness of the iodine prophylaxis model adopted in Poland.

Iodine deficiency disorders incidence in neonates based on the experience with mass screening for congenital hypothyroidism in southeast Poland in the years 1985-2000.

Comparative analysis of zinc status, food products' frequency intake and food habits of 11-year-old healthy children.

[Molecular studies in a population of children with bronchial asthma. I. Polymorphism in the promotor region of gene CD14].

The influence of lead and cadmium environmental pollution on anthropometric health factors in children.

Macroprolactinoma with an atypical course.

Impact of the use of Extended™ Wear Infusion sets on metabolic, ultrasound, and psychological outcomes in adults with type 1 diabetes using the Medtronic MiniMed 780G: a pilot randomized controlled trial.

The association between abdominal muscle mass quantified by computed tomography and osteoporosis in postmenopausal women.

Beyond traditional biopsy: integrating liquid biopsy, molecular panels, and advanced imaging techniques in thyroid cancer management.

Estimating obesity phenotype features in a real-world cohort - a non-interventional pilot study using an original questionnaire.

Type 5 diabetes mellitus: revisiting malnutrition-related diabetes.

Intrafamilial phenotypic variation in four Palestinian siblings with CFAP418-related ciliopathy: a familial case series.

Genetic variants in NEF2L2 rs35652124 and GABRB3 rs2081648 genes: association with autism spectrum disorder in Iraqi children.

Phenotypic spectrum of 1q21.1 copy number variants in 42 children: genotype-phenotype correlations and clinical implications.

Estimating the Heritability of Intelligence with a Nuclear Twin Family Design.

Gut microbiota and the gut-brain axis in autism spectrum disorder and attention-deficit/hyperactivity disorder: A scoping review of shared and disorder-specific mechanistic pathways.

Case Report: Neonatal lethality caused by novel compound heterozygous missense variants of SLC6A9 gene.

Related Experiment Videos

[Genetic basis of familial multihormonal hypothalamo-hypophyseal dwarfism in children]

Related Concept Videos

Related Articles