[Familial form of saccharase deficiency]

First-line immunosuppressive treatment in children with aplastic anemia: rabbit antithymocyte globulin.

Advances in experimental medicine and biology·2014

Diagnosis and treatment of renal cell carcinoma in children: a report from the Polish pediatric rare tumor study group.

Klinische Padiatrie·2011

Serum soluble interleukin-2 receptor, beta2-microglobulin, lactate dehydrogenase and erythrocyte sedimentation rate in children with Hodgkin's lymphoma.

Scandinavian journal of immunology·2009

Angiosarcoma in children - still uncontrollable oncological problem. The report of the Polish Paediatric Rare Tumours Study.

European journal of cancer care·2009

Interleukin-12 and tumour necrosis factor-alpha equilibrium is a prerequisite for clinical course free from late complications in children with type 1 diabetes mellitus.

Scandinavian journal of immunology·2008

Serum soluble interleukin 2 receptor alpha in human cancer of adults and children: a review.

Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals·2007

Monoclonal antibodies for prophylactic and therapeutic use against viral infections.

Pediatria polska·2020

[Barriers in breast feeding: contraindications].

Pediatria polska·1996

[Echinococcosis infection in three children].

Pediatria polska·1996

[Newborn baby with extreme acidosis].

Pediatria polska·1996

[Adult stature prediction in boys according to the Khamis-Roche method and proposed regression equations].

Pediatria polska·1996

[Serum prolactin concentration in children with celiac disease].

Pediatria polska·1996

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

[Familial form of saccharase deficiency]

Related Concept Videos

First-line immunosuppressive treatment in children with aplastic anemia: rabbit antithymocyte globulin.

Diagnosis and treatment of renal cell carcinoma in children: a report from the Polish pediatric rare tumor study group.

Serum soluble interleukin-2 receptor, beta2-microglobulin, lactate dehydrogenase and erythrocyte sedimentation rate in children with Hodgkin's lymphoma.

Angiosarcoma in children - still uncontrollable oncological problem. The report of the Polish Paediatric Rare Tumours Study.

Interleukin-12 and tumour necrosis factor-alpha equilibrium is a prerequisite for clinical course free from late complications in children with type 1 diabetes mellitus.

Serum soluble interleukin 2 receptor alpha in human cancer of adults and children: a review.

Monoclonal antibodies for prophylactic and therapeutic use against viral infections.

[Barriers in breast feeding: contraindications].

[Echinococcosis infection in three children].

[Newborn baby with extreme acidosis].

[Adult stature prediction in boys according to the Khamis-Roche method and proposed regression equations].

[Serum prolactin concentration in children with celiac disease].

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

[Familial form of saccharase deficiency]

Related Concept Videos

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