Justyna Paprocka

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing

Sharita Timal, Alexander Hoischen, Ludwig Lehle et al. · Human Molecular Genetics · 2012 · 170 citations

Mendelian Disorder, Genetic Disorder, Whole-exome Sequencing +14

CDKL5 Deficiency Disorder—A Complex Epileptic Encephalopathy

Martyna Jakimiec, Justyna Paprocka, Robert Śmigiel · Brain Sciences · 2020 · 92 citations · Full text

Megalencephalic leukoencephalopathy with subcortical cysts

Eline M. Hamilton, Pınar Tektürk, Fia Cialdella et al. · Neurology · 2018 · 81 citations · Full text

Difficulties in differentiation of Parry–Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome

Justyna Paprocka, Ewa Jamroz, Dariusz Adamek et al. · Child s Nervous System · 2005 · 76 citations

Rasmussen Syndrome, Unilateral Facial Sclerodermia, Scleroderma +9

Eating Behaviors of Children with Autism—Pilot Study

Anna Brzóska, Beata Kazek, Karolina Kozioł et al. · Nutrients · 2021 · 37 citations · Full text