[Case of Münchmeyer's syndrome (myositis ossificans progressiva)]

Warburg micro syndrome type 1 associated with peripheral neuropathy and cardiomyopathy.

Folia neuropathologica·2016

Pelizaeus-Merzbacher disease in patients with molecularly confirmed diagnosis.

Folia neuropathologica·2016

Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation - a novel phenotype of the mitochondrial disease.

Clinical genetics·2016

Molecular and clinical consequences of novel mutations in the arylsulfatase A gene.

Clinical genetics·2008

Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls.

Journal of inherited metabolic disease·2007

[Clinical picture of spinocerebellar ataxia type I (SCA1)].

Neurologia i neurochirurgia polska·2002

[Tuberculosis of the lymph nodes with esophageal-cutaneous fistula in a patient with AIDS].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

[Multiorgan changes in AIDS in a reported case].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

[Efficacy of cimetidine in treatment of Herpes zoster in the first 5 days from the moment of disease manifestation].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

[Antibody avidity in diagnosis of toxoplasmosis].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

[The effect of discontinuing intravenous opiate injections and methadone treatment on the status of the immune system in narcotic abusers with HIV].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

[Use of human anti-Pseudomonas immunoglobulins in treatment of children with burns].

Polski tygodnik lekarski (Warsaw, Poland : 1960)·1996

Association of doxycycline treatment with time to first documented MP-RNA negative conversion in pediatric Mycoplasma pneumoniae pneumonia: a retrospective cohort study.

Italian journal of pediatrics·2026

Anatomical location defines distinct molecular subtypes of mucosal melanoma.

ESMO open·2026

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Human molecular genetics·2026

Meissnerian neurofibroma: A rare histological variant of neurofibroma.

Indian journal of pathology & microbiology·2026

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

The Journal of experimental medicine·2026

Acidic Stress Induces Proteomic Reprogramming and Virulence-Associated Adaptation in Paracoccidioides brasiliensis.

Journal of proteome research·2026

Related Experiment Videos

[Case of Münchmeyer's syndrome (myositis ossificans progressiva)]

Related Concept Videos

Warburg micro syndrome type 1 associated with peripheral neuropathy and cardiomyopathy.

Pelizaeus-Merzbacher disease in patients with molecularly confirmed diagnosis.

Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation - a novel phenotype of the mitochondrial disease.

Molecular and clinical consequences of novel mutations in the arylsulfatase A gene.

Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls.

[Clinical picture of spinocerebellar ataxia type I (SCA1)].

[Tuberculosis of the lymph nodes with esophageal-cutaneous fistula in a patient with AIDS].

[Multiorgan changes in AIDS in a reported case].

[Efficacy of cimetidine in treatment of Herpes zoster in the first 5 days from the moment of disease manifestation].

[Antibody avidity in diagnosis of toxoplasmosis].

[The effect of discontinuing intravenous opiate injections and methadone treatment on the status of the immune system in narcotic abusers with HIV].

[Use of human anti-Pseudomonas immunoglobulins in treatment of children with burns].

Association of doxycycline treatment with time to first documented MP-RNA negative conversion in pediatric Mycoplasma pneumoniae pneumonia: a retrospective cohort study.

Anatomical location defines distinct molecular subtypes of mucosal melanoma.

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Meissnerian neurofibroma: A rare histological variant of neurofibroma.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Acidic Stress Induces Proteomic Reprogramming and Virulence-Associated Adaptation in Paracoccidioides brasiliensis.

Related Experiment Videos

[Case of Münchmeyer's syndrome (myositis ossificans progressiva)]

Related Concept Videos

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