[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

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·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].

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

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[Familial form of saccharase deficiency]

Related Concept Videos

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