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Patryk Lipiński

Showing results (1-10 of 67) with videos related to

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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 ChildrenPatryk Lipiński, Anna Doroba
Postepy Biochemii|December 15, 2020
Congenital disorder of deglycosylation associated with N-glycanse 1 deficiencyPatryk Lipiński, Anna Tylki-Szymańska
Postepy Biochemii|December 11, 2021
Disturbance of lipid homeostasis in lysosomal lipase deficiency – pathomechanism, diagnosis and treatmentPatryk Lipiński, Anna Tylki-Szymańska
Diagnostics (Basel, Switzerland)|June 27, 2024
The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and TreatmentPatryk 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 studyJolanta 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 populationPatryk Lipiński, Anna Bogdańska, Anna Tylki-Szymańska
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 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 ChildrenPatryk Lipiński, Anna Doroba
Postepy Biochemii|December 15, 2020
Congenital disorder of deglycosylation associated with N-glycanse 1 deficiencyPatryk Lipiński, Anna Tylki-Szymańska
Postepy Biochemii|December 11, 2021
Disturbance of lipid homeostasis in lysosomal lipase deficiency – pathomechanism, diagnosis and treatmentPatryk Lipiński, Anna Tylki-Szymańska
Diagnostics (Basel, Switzerland)|June 27, 2024
The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and TreatmentPatryk 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 studyJolanta 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 populationPatryk Lipiński, Anna Bogdańska, Anna Tylki-Szymańska
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