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Author/Creator Pawłowicz, Małgorzata

1. Coincidence of PTPN22 c.1858CC and FCRL3 ‐169CC genotypes as a biomarker of preserved residual β‐cell function in children with type 1 diabetes12. Issue 8 (12th September 2016)

Authors:
Pawłowicz, Małgorzata; Filipów, Rafał; Krzykowski, Grzegorz; Stanisławska‐Sachadyn, Anna; Morzuch, Lucyna; Kulczycka, Julia; Balcerska, Anna; Limon, Janusz
Journal:
Pediatric diabetes
Issue:
Volume 18:Issue 8(2017)
Page Start:
696
Record Type:
Journal Article
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3. Expanding the phenotype of DNAJC30‐associated Leigh syndrome. Issue 5 (29th July 2022)

Authors:
Zawadzka, Marta; Krygier, Magdalena; Pawłowicz, Małgorzata; Wilke, Matheus Vernet Machado Bressan; Rutkowska, Karolina; Gueguen, Naig; Desquiret‐Dumas, Valerie; Klee, Eric W.; Schimmenti, Lisa A.; Sławek, Jarosław; Procaccio, Vincent; Płoski, Rafał; Mazurkiewicz‐Bełdzińska, Maria
Journal:
Clinical genetics
Issue:
Volume 102:Issue 5(2022)
Page Start:
438
Record Type:
Journal Article
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4. The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy. Issue 22 (23rd October 2022)

Authors:
Fogarasi, Andras; Fazzi, Elisa; Smorenburg, Ana R. P.; Mazurkiewicz-Beldzinska, Maria; Dinopoulos, Argirios; Pobiecka, Alena; Schröder-van den Nieuwendijk, Dea; Kraus, Josef; Tekgül, Hasan; Kraus, Josef; Dinopoulos, Argirios; Koutsaki, Maria; Fogarasi, Andras; Baranello, Giovanni; Bertoli, Simona...
Journal:
Disability and rehabilitation
Issue:
Volume 44:Issue 22(2022)
Page Start:
6668
Record Type:
Journal Article
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