Patryk Lipinski

Dziekanow Lesny, MZ, Poland

Last Updated: 09/26/2026

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Found 71 publications

Vaccination of children with inborn errors of metabolism: safety, immunogenicity, and practical implications.

Vaccination of children with inborn errors of metabolism: safety, immunogenicity, and practical implications.

Journal: European journal of pediatrics

Published: July 23, 2026

Safety and Efficacy of Ambroxol Therapy in Polish Patients with Gaucher Disease.

Safety and Efficacy of Ambroxol Therapy in Polish Patients with Gaucher Disease.

Journal: Life (Basel, Switzerland)

Published: January 09, 2026

The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in Children.

The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in Children.

Journal: Diagnostics (Basel, Switzerland)

Published: September 13, 2025

Mucopolysaccharidoses-What Clinicians Need to Know: A Clinical, Biochemical, and Molecular Overview.

Mucopolysaccharidoses-What Clinicians Need to Know: A Clinical, Biochemical, and Molecular Overview.

Journal: Biomolecules

Published: September 04, 2025

Alpha-methylacyl-CoA racemase (AMACR) deficiency: report on novel patient and literature review.

Alpha-methylacyl-CoA racemase (AMACR) deficiency: report on novel patient and literature review.

Journal: Journal of applied genetics

Published: July 07, 2025

Urolithiasis in Children-Clinical Picture, Pathogenesis, and Diagnostic Approach.

Urolithiasis in Children-Clinical Picture, Pathogenesis, and Diagnostic Approach.

Journal: Biomolecules

Published: June 29, 2025

Approach to a Child with Hypophosphatemia.

Approach to a Child with Hypophosphatemia.

Journal: Biomolecules

Published: June 26, 2025

Autism spectrum disorder and inherited metabolic diseases: are there any common features?

Autism spectrum disorder and inherited metabolic diseases: are there any common features?

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: May 12, 2025

Hypophosphatasia in children: From low alkaline phosphatase activity to diagnosis, genetic testing, and treatment options. A narrative review.

Hypophosphatasia in children: From low alkaline phosphatase activity to diagnosis, genetic testing, and treatment options. A narrative review.

Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University

Published: April 15, 2025

Maternal Uniparental Isodisomy of Chromosome 6: A Novel Case of Teratoma and Autism Spectrum Disorder with a Diagnostic and Management Framework.

Maternal Uniparental Isodisomy of Chromosome 6: A Novel Case of Teratoma and Autism Spectrum Disorder with a Diagnostic and Management Framework.

Journal: Genes

Published: February 24, 2025

Riboflavin treatment in L-2-hydroxyglutaric aciduria: report on a pediatric patient and literature review.

Riboflavin treatment in L-2-hydroxyglutaric aciduria: report on a pediatric patient and literature review.

Journal: Journal of applied genetics

Published: February 05, 2025

Effects of GBA1 Variants and Prenatal Exposition on the Glucosylsphingosine (Lyso-Gb1) Levels in Gaucher Disease Carriers.

Effects of GBA1 Variants and Prenatal Exposition on the Glucosylsphingosine (Lyso-Gb1) Levels in Gaucher Disease Carriers.

Journal: International journal of molecular sciences

Published: October 08, 2024

Showing 1-12 of 71

Last Updated: 09/26/2026