Get started
Author

Łukasz Pawliński

Observed names: L. Pawlinski, LUKASZ PAWLINSKI, Lukasz Pawlinski
ORCID: 0000-0002-2743-1922
Observed ORCID: 0000-0002-2743-1922
OpenAlex ID: A5024511024
Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation
2020 · Anna Čechová, Ruqaiah Altassan, et al. · Journal of Inherited Metabolic Disease · 67
PDF
Neurological symptoms in hospitalised patients with COVID-19 and their association with in-hospital mortality
2021 · Marcin Wnuk, Katarzyna Sawczyńska, et al. · Neurologia i Neurochirurgia Polska · 28
PDF
The additive effect on the antiepileptic treatment of ambroxol in type 3 Gaucher patient. The early observation
2016 · Lukasz Pawlinski, Maciej T Malecki, et al. · Blood Cells Molecules and Diseases · 21
Epigenetic mechanism in search for the pathomechanism of diabetic neuropathy development in diabetes mellitus type 1 (T1DM)
2020 · Joanna Gastoł, Przemysław Kapusta, et al. · Endocrine · 20
Dual‐action ambroxol in treatment of chronic pain in Gaucher Disease
2020 · Lukasz Pawlinski, Magdalena Krawczyk, et al. · European Journal of Pain · 12
Proteomic biomarkers in Gaucher disease
2020 · Łukasz Pawliński, Ewa Tobór, et al. · Journal of Clinical Pathology · 11
Specific gene expression in type 1 diabetic patients with and without cardiac autonomic neuropathy
2020 · Joanna Gastol, Anna Polus, et al. · Scientific Reports · 8
Gene expression with corresponding pathways analysis in Gaucher disease
2021 · Łukasz Pawliński, Anna Polus, et al. · Experimental and Molecular Pathology · 6
Case report of endoprosthesis -Y implantation in severe respiratory failure in the MPSII patient; comparison with literature data
2020 · Wojciech Gocyk, Janusz Warmus, et al. · BMC Pulmonary Medicine · 6
PDF
Is treatment of type 1 diabetes mellitus (insulin therapy, metabolic control) optimal for preventing cardiovascular autonomic neuropathy?
2019 · Łukasz Pawliński, Joanna Gastoł, et al. · Endokrynologia Polska · 6
PDF
MiRNA Expression in Patients with Gaucher Disease Treated with Enzyme Replacement Therapy
2020 · Łukasz Pawliński, Anna Polus, et al. · Life · 4
The Complexities of Diagnosis with Co-Existing Gaucher Disease and Hemato-Oncology—A Case Report and Review of the Literature
2023 · Paulina Sudul, Beata Piatkowska-Jakubas, et al. · Journal of Clinical Medicine · 3
Diagnostic delay in inherited metabolic diseases: Insights from the U-IMD registry
2026 · Julian Teinert, Florian Gleich, et al. · Genetics in Medicine · 2
Trappsol®Cyclo™ and NPC: Efficacy shown across individual 5D domains and utilization of future assessment tools to demonstrate clinically relevant outcomes
2025 · Caroline A. Hastings, Fatih S. Ezgu, et al. · Molecular Genetics and Metabolism · 1
[Cardiovascular autonomic neuropathy in the course of diabetes - the review of actual knowledge.]
2019 · Beata Kieć-Wilk, Joanna Gastoł, et al. · PubMed · 1
Neuropatia autonomiczna układu sercowo-naczyniowego w przebiegu cukrzycy - aktualny stan wiedzy.
2019 · Beata Kieć-Wilk, Joanna Gastoł, et al. · Postępy Biochemii · 1
Primary care providers-initiated screening for familial hypercholesterolemia: a model proposed based on the Kordian primary prevention program for cardiovascular diseases
2026 · Beata Bobrowska, Renata Rajtar-Salwa, et al. · Polskie Archiwum Medycyny Wewnętrznej
PDF
A pioneering transition program for adults with phenylketonuria – initial findings from a single-center one-year experience from Poland
2026 · Michal Kania, Martyna Pietruś, et al. · Clinics
PDF
1323-P: Glycemic Status of Adult Patients with Phenylketonuria—Preliminary Data from a Pilot Study
2025 · MICHAL KANIA, LUKASZ PAWLINSKI, et al. · Diabetes
Trappsol® Cyclo™ (hpβCd) for the long-term treatment of Niemann Pick type C1: Efficacy and safety data from 4 clinical studies and the ongoing expanded access program
2025 · Caroline A. Hastings, Fatih S. Ezgu, et al. · Molecular Genetics and Metabolism
I suffer from several serious diseases”. The Dunnigan-type of familial partial lipodystrophy: a multiple-symptom disorder caused by genetic mutation
2025 · Magdalena Płonka-Stępień, Jerzy Hohendorff, et al. · Polskie Archiwum Medycyny Wewnętrznej
PDF
Osteoarticular changes in Refsum’s disease: a case report
2023 · Marcin Bednarek, Maciej Belka, et al. · Research Square
PDF
545-P: Posttranslation Control Mechanisms (miRNAs) in Type 1 Diabetic Patients with and without Cardiac Autonomic Neuropathy
2020 · EWA TOBOR, ANNA POLUS, et al. · Diabetes
Serum triglyceride levels are associated with cytokeratin –18 concentration in patients with type 2 diabetes and non-alcoholic fatty liver disease.
2014 · M. Walus-Miarka, A. Trojak, et al. · Atherosclerosis
Works count: 25
Citation count: 197
H-index: 7
I10-index: 6
Year
Topic
Type