List of works - Věra Malinová

1H MR spectroscopy as a diagnostic tool for cerebral creatine deficiency

scientific article published on 26 August 2008

A prospective study in children with a severe form of atopic dermatitis: clinical outcome in relation to cytokine gene polymorphisms

scientific article published on January 1, 2012

Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature

scientific article

Cataplexy and sleep disorders in Niemann-Pick type C disease

scientific article published on January 2015

Clinical Effect And Safety Profile of Recombinant Human Lysosomal Acid Lipase in Patients With Cholesteryl Ester Storage Disease ⬇️

scientific article published on March 28, 2013

Clinical Features of Lysosomal Acid Lipase Deficiency

scientific article

Effect of rapid cessation of enzyme replacement therapy: a report of 5 more cases

scientific article published on 06 September 2013

Enzyme replacement therapy for Gaucher disease in twin pregnancy

scientific article published on 05 April 2009

Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe.

scientific article

Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases.

scientific article

Sebelipase Alfa for Lysosomal Acid Lipase Deficiency: 5-Year Treatment Experience From a Phase 2 Open-Label Extension Study

scientific article published on 13 July 2020

Sebelipase alfa over 52 weeks reduces serum transaminases, liver volume and improves serum lipids in patients with lysosomal acid lipase deficiency

scientific article

Serum immunoglobulin free light chains in severe forms of atopic dermatitis

scientific article published on 01 April 2010

The female Gaucher patient: the impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause).

scientific article published on 06 June 2009

[A case of Pelger-Huet anomaly in a premature infant]

scientific article published on 01 January 1989

[Enzyme therapy in children with severe forms of Gaucher's disease]

scientific article published on 01 February 1997

List of works by Věra Malinová

1H MR spectroscopy as a diagnostic tool for cerebral creatine deficiency

A prospective study in children with a severe form of atopic dermatitis: clinical outcome in relation to cytokine gene polymorphisms

Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature

Cataplexy and sleep disorders in Niemann-Pick type C disease

Clinical Effect And Safety Profile of Recombinant Human Lysosomal Acid Lipase in Patients With Cholesteryl Ester Storage Disease ⬇️

Clinical Features of Lysosomal Acid Lipase Deficiency

Effect of rapid cessation of enzyme replacement therapy: a report of 5 more cases

Enzyme replacement therapy for Gaucher disease in twin pregnancy

Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe.

Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases.

Sebelipase Alfa for Lysosomal Acid Lipase Deficiency: 5-Year Treatment Experience From a Phase 2 Open-Label Extension Study

Sebelipase alfa over 52 weeks reduces serum transaminases, liver volume and improves serum lipids in patients with lysosomal acid lipase deficiency

Serum immunoglobulin free light chains in severe forms of atopic dermatitis

The female Gaucher patient: the impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause).

[A case of Pelger-Huet anomaly in a premature infant]

[Enzyme therapy in children with severe forms of Gaucher's disease]