[Growth hormone and prolactin levels in patients with Horton's headache]

[Globoid cell leukodystrophy of adult. A first case in Poland].

Neurologia i neurochirurgia polska·2013

A randomized, double-blind, placebo-controlled, parallel-group, enriched-design study of nabiximols* (Sativex(®) ), as add-on therapy, in subjects with refractory spasticity caused by multiple sclerosis.

European journal of neurology·2011

Activity of selected enzymes in erythrocytes and level of plasma antioxidants in response to single whole-body cryostimulation in humans.

Scandinavian journal of clinical and laboratory investigation·2009

[SUNCT syndrome--case report].

Neurologia i neurochirurgia polska·2001

[Night headache: report of 2 cases].

Neurologia i neurochirurgia polska·2000

[The myasthenic syndrome after chloroquine].

Neurologia i neurochirurgia polska·1999

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

Hypophosphatemic rickets in children: current knowledge and a proposal for a diagnostic algorithm.

Endokrynologia Polska·2026

Association between Helicobacter pylori infection and hyperandrogenism in women with polycystic ovary syndrome.

Endokrynologia Polska·2026

Hematological changes in Cushing's disease from diagnosis to remission: comparison with non-functioning pituitary adenomas.

Endokrynologia Polska·2026

Assessment of phenotypes in a unique group of RET proto-oncogene Y791F variant carriers in the Polish population.

Endokrynologia Polska·2026

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

Related Experiment Videos

[Growth hormone and prolactin levels in patients with Horton's headache]

Related Concept Videos

[Globoid cell leukodystrophy of adult. A first case in Poland].

A randomized, double-blind, placebo-controlled, parallel-group, enriched-design study of nabiximols* (Sativex(®) ), as add-on therapy, in subjects with refractory spasticity caused by multiple sclerosis.

Activity of selected enzymes in erythrocytes and level of plasma antioxidants in response to single whole-body cryostimulation in humans.

[SUNCT syndrome--case report].

[Night headache: report of 2 cases].

[The myasthenic syndrome after chloroquine].

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.

Hypophosphatemic rickets in children: current knowledge and a proposal for a diagnostic algorithm.

Association between Helicobacter pylori infection and hyperandrogenism in women with polycystic ovary syndrome.

Hematological changes in Cushing's disease from diagnosis to remission: comparison with non-functioning pituitary adenomas.

Assessment of phenotypes in a unique group of RET proto-oncogene Y791F variant carriers in the Polish population.

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Familial short stature: genetic architecture, risk stratification, and precision management.

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Related Experiment Videos

[Growth hormone and prolactin levels in patients with Horton's headache]

Related Concept Videos

Related Articles