Search research articles
Contact Us
Filters
Showing results (1-10 of 67) with videos related to
Page
of 7
Sort By:
Pediatric Endocrinology, Diabetes, and Metabolism
|
May 12, 2025
Autism spectrum disorder and inherited metabolic diseases: are there any common features?
Patryk Lipiński
Developmental Period Medicine
|
January 14, 2019
[Progressive familial intrahepatic cholestasis type 3]
Patryk Lipiński, Irena Jankowska
Diagnostics (Basel, Switzerland)
|
November 13, 2025
The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in Children
Patryk Lipiński, Anna Doroba
Postepy Biochemii
|
December 15, 2020
Congenital disorder of deglycosylation associated with N-glycanse 1 deficiency
Patryk Lipiński, Anna Tylki-Szymańska
Postepy Biochemii
|
December 11, 2021
Disturbance of lipid homeostasis in lysosomal lipase deficiency – pathomechanism, diagnosis and treatment
Patryk Lipiński, Anna Tylki-Szymańska
Diagnostics (Basel, Switzerland)
|
June 27, 2024
The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and Treatment
Patryk Lipiński, Anna Tylki-Szymańska
Frontiers in Pediatrics
|
September 20, 2021
Congenital Disorders of Glycosylation: What Clinicians Need to Know?
Patryk Lipiński, Anna Tylki-Szymańska
Acta Biochimica Polonica
|
February 28, 2022
Efficacy of Enzyme Replacement Therapy on the range of motion of the upper and lower extremities in 16 Polish patients with mucopolysaccharidosis type II: A long-term follow-up study
Jolanta Marucha, Patryk Lipiński, Anna Tylki-Szymańska
Developmental Period Medicine
|
July 30, 2018
[Transaldolase deficiency - clinical outcome, pathogenesis, diagnostic process]
Patryk Lipiński, Teresa Stradomska, Anna Tylki-Szymańska
Molecular Genetics and Metabolism Reports
|
March 1, 2021
Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population
Patryk Lipiński, Anna Bogdańska, Anna Tylki-Szymańska
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Pediatric Endocrinology, Diabetes, and Metabolism
|
May 12, 2025
Autism spectrum disorder and inherited metabolic diseases: are there any common features?
Patryk Lipiński
Developmental Period Medicine
|
January 14, 2019
[Progressive familial intrahepatic cholestasis type 3]
Patryk Lipiński, Irena Jankowska
Diagnostics (Basel, Switzerland)
|
November 13, 2025
The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in Children
Patryk Lipiński, Anna Doroba
Postepy Biochemii
|
December 15, 2020
Congenital disorder of deglycosylation associated with N-glycanse 1 deficiency
Patryk Lipiński, Anna Tylki-Szymańska
Postepy Biochemii
|
December 11, 2021
Disturbance of lipid homeostasis in lysosomal lipase deficiency – pathomechanism, diagnosis and treatment
Patryk Lipiński, Anna Tylki-Szymańska
Diagnostics (Basel, Switzerland)
|
June 27, 2024
The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and Treatment
Patryk Lipiński, Anna Tylki-Szymańska
Frontiers in Pediatrics
|
September 20, 2021
Congenital Disorders of Glycosylation: What Clinicians Need to Know?
Patryk Lipiński, Anna Tylki-Szymańska
Acta Biochimica Polonica
|
February 28, 2022
Efficacy of Enzyme Replacement Therapy on the range of motion of the upper and lower extremities in 16 Polish patients with mucopolysaccharidosis type II: A long-term follow-up study
Jolanta Marucha, Patryk Lipiński, Anna Tylki-Szymańska
Developmental Period Medicine
|
July 30, 2018
[Transaldolase deficiency - clinical outcome, pathogenesis, diagnostic process]
Patryk Lipiński, Teresa Stradomska, Anna Tylki-Szymańska
Molecular Genetics and Metabolism Reports
|
March 1, 2021
Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population
Patryk Lipiński, Anna Bogdańska, Anna Tylki-Szymańska
Page
of 7