[Genetic advice for hereditary diseases of monogenetic origin (author's transl)]

Tocilizumab and immune signatures for targeted management of cytokine release syndrome in immune checkpoint therapy.

Annals of oncology : official journal of the European Society for Medical Oncology·2024

[Myelodysplastic syndromes and autoimmunity].

Revue medicale suisse·2015

Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model.

Nature communications·2014

Core-shell inversion by pH modulation in dynamic covalent micelles.

Soft matter·2014

Rodlike complexes of a polyelectrolyte (hyaluronan) and a protein (lysozyme) observed by SANS.

Biomacromolecules·2011

Cooling and freezing of epididymal sperm in the common hippopotamus (Hippopotamus amphibius).

Theriogenology·2010

[Neuroendocrine tumors of the stomach (stomach carcinoid)].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

[Time of drug intake in hypertension and angina pectoris. A controlled monitoring study].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

[Mental suffering IN patients with parkinsonism].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

[Liver transplantation 1994].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

[Diagnosis and therapy of portosystemic encephalopathy].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

[Ascites].

Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis·1994

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Clinical laboratory·2026

Audiological Features in Pendred Syndrome: A Scoping Review.

The journal of international advanced otology·2026

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Frontiers in endocrinology·2026

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Frontiers in psychiatry·2026

Related Experiment Videos

[Genetic advice for hereditary diseases of monogenetic origin (author's transl)]

Related Concept Videos

Tocilizumab and immune signatures for targeted management of cytokine release syndrome in immune checkpoint therapy.

[Myelodysplastic syndromes and autoimmunity].

Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model.

Core-shell inversion by pH modulation in dynamic covalent micelles.

Rodlike complexes of a polyelectrolyte (hyaluronan) and a protein (lysozyme) observed by SANS.

Cooling and freezing of epididymal sperm in the common hippopotamus (Hippopotamus amphibius).

[Neuroendocrine tumors of the stomach (stomach carcinoid)].

[Time of drug intake in hypertension and angina pectoris. A controlled monitoring study].

[Mental suffering IN patients with parkinsonism].

[Liver transplantation 1994].

[Diagnosis and therapy of portosystemic encephalopathy].

[Ascites].

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Audiological Features in Pendred Syndrome: A Scoping Review.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Related Experiment Videos

[Genetic advice for hereditary diseases of monogenetic origin (author's transl)]

Related Concept Videos

Related Articles