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Author/Creator Winczewska-Wiktor, Anna

1. A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report. Issue 1 (December 2016)

Authors:
Winczewska-Wiktor, Anna; Badura-Stronka, Magdalena; Monies-Nowicka, Anna; Nowicki, Michal; Steinborn, Barbara; Latos-Bieleńska, Anna; Monies, Dorota
Journal:
BMC neurology
Issue:
Volume 16:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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2. Phenotype of two Polish patients with Schaaf–Yang syndrome confirmed by identifying mutation in MAGEL2 gene. Issue 2 (April 2018)

Authors:
Matuszewska, Karolina E.; Badura-Stronka, Magdalena; Śmigiel, Robert; Cabała, Magdalena; Biernacka, Anna; Kosinska, Joanna; Rydzanicz, Malgorzata; Winczewska-Wiktor, Anna; Sasiadek, Maria; Latos-Bieleńska, Anna; Żemojtel, Tomasz; Płoski, Rafal
Journal:
Clinical dysmorphology
Issue:
Volume 27:Issue 2(2018:Apr.)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. 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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Available online (eLD content is only available in our Reading Rooms) ↗