Maciej R Krawczynski (Maciej Krawczyński, Maciej R Krawczyński)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 17

Top Venues

Metabolic brain disease

International journal of molecular sciences

Diagnostics (Basel, Switzerland)

Biomedicines

Poznan University of Medical Sciences

Poznan University of Medical Sciences (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Poznan University of Medical Sciences Oct 01 1991

Poland

Assistant, Assistant Professor, Asociate Professor, Full Professor :: Department of Medical Genetics

Education History

Poznan University of Medical Sciences Oct 01 1994 - Feb 12 1997

Poland

PHD :: Department of Medical Genetics

Publications

Anna Wawrocka, Joanna Walczak-Sztulpa, Łukasz Kuszel, Zuzanna Niedziela-Schwartz, Anna Skorczyk-Werner, Jadwiga Bernardczyk-Meller, Maciej R Krawczynski
Coexistence of Retinitis Pigmentosa and Ataxia in Patients with PHARC, PCARP, and Oliver-McFarlane Syndromes. International journal of molecular sciences 25 (11) (2024)
Ewa Matczyńska, Marta Beć-Gajowniczek, Larysa Sivitskaya, Elżbieta Gregorczyk, Przemysław Łyszkiewicz, Robert Szymańczak, Maria Jędrzejowska, Edward Wylęgała, Maciej R Krawczynski, Sławomir Jan Teper, Anna Boguszewska-Chachulska
Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland. Biomedicines 12 (6) (2024)
Ewa Matczyńska, Marta Beć-Gajowniczek, Larysa Sivitskaya, Elżbieta Gregorczyk, Przemysław Łyszkiewicz, Robert Szymańczak, Maria Jędrzejowska, Edward Wylęgała, Maciej R Krawczynski, Sławomir Jan Teper, Anna Boguszewska-Chachulska
Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland. Biomedicines 12 (6) (2024)
Anna Wawrocka, Joanna Walczak-Sztulpa, Łukasz Kuszel, Zuzanna Niedziela-Schwartz, Anna Skorczyk-Werner, Jadwiga Bernardczyk-Meller, Maciej R Krawczynski
Coexistence of Retinitis Pigmentosa and Ataxia in Patients with PHARC, PCARP, and Oliver-McFarlane Syndromes. International journal of molecular sciences 25 (11) (2024)
Anna Skorczyk-Werner, Katarzyna Tońska, Aleksandra Maciejczuk, Katarzyna Nowomiejska, Magdalena Korwin, Monika Ołdak, Anna Wawrocka, Maciej R Krawczynski
DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients. International journal of molecular sciences 24 (24) (2023)
Anna Wawrocka, Magdalena Socha, Joanna Walczak-Sztulpa, Grzegorz Koczyk, Anna Skorczyk-Werner, Maciej R Krawczynski
Molecular Re-Diagnosis with Whole-Exome Sequencing Increases the Diagnostic Yield in Patients with Non-Syndromic Retinitis Pigmentosa. Diagnostics (Basel, Switzerland) 13 (4) (2023)
Anna Wawrocka, Magdalena Socha, Joanna Walczak-Sztulpa, Grzegorz Koczyk, Anna Skorczyk-Werner, Maciej R Krawczynski
Molecular Re-Diagnosis with Whole-Exome Sequencing Increases the Diagnostic Yield in Patients with Non-Syndromic Retinitis Pigmentosa. Diagnostics (Basel, Switzerland) 13 (4) (2023)
Anna Skorczyk-Werner, Katarzyna Tońska, Aleksandra Maciejczuk, Katarzyna Nowomiejska, Magdalena Korwin, Monika Ołdak, Anna Wawrocka, Maciej R Krawczynski
DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients. International journal of molecular sciences 24 (24) (2023)
Anna Wawrocka, Magdalena Socha, Joanna Walczak-Sztulpa, Grzegorz Koczyk, Anna Skorczyk-Werner, Maciej R Krawczynski
Molecular Re-Diagnosis with Whole-Exome Sequencing Increases the Diagnostic Yield in Patients with Non-Syndromic Retinitis Pigmentosa. Diagnostics (Basel, Switzerland) 13 (4) (2023)
Anna Skorczyk-Werner, Katarzyna Tońska, Aleksandra Maciejczuk, Katarzyna Nowomiejska, Magdalena Korwin, Monika Ołdak, Anna Wawrocka, Maciej R Krawczynski
DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients. International journal of molecular sciences 24 (24) (2023)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease 38 (2) (2022)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease 38 (2) (2022)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease (2022)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease 38 (2) (2022)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease 38 (2) (2022)
Joanna Karolina Purzycka-Olewiecka, Katarzyna Hetmańczyk-Sawicka, Tomasz Kmieć, Dominika Szczęśniak, Joanna Trubicka, Maciej R Krawczynski, Maciej Pronicki, Agnieszka Ługowska
Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic brain disease 38 (2) (2022)
Agnieszka Piotrowska-Nowak, Maciej R Krawczynski, Ewa Kosior-Jarecka, Anna M Ambroziak, Magdalena Korwin, Monika Ołdak, Katarzyna Tońska, Ewa Bartnik
Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation. Metabolic brain disease 35 (8) (2020)

Maciej R Krawczynski.css-eqlu8i{font-size:small;padding-left:4px;} (Maciej Krawczyński, Maciej R Krawczyński)

Publication Activity (10 Years)

Top Topics

Top Venues

Maciej R Krawczynski (Maciej Krawczyński, Maciej R Krawczyński)