Karin Writzl

Hallmarks of aging: An expanding universe

Red cell pyruvate kinase deficiency: molecular and clinical aspects

Cancer stem cells revisited

Pathophysiology of premature aging characteristics in Mendelian progeroid disorders

Fluorescence nanoscopy in cell biology

Fatty acylation of Wnt proteins

22q11.2 deletion syndrome

Mechanisms of Cell Protection by Heme Oxygenase-1

CHARGE (Coloboma, Heart Defect, Atresia Choanae, Retarded Growth and Development, Genital Hypoplasia, Ear Anomalies/Deafness) Syndrome and Chromosome 22q11.2 Deletion Syndrome: A Comparison of Immunologic and Nonimmunologic Phenotypic Features

Developmental mechanism of the periodic membrane skeleton in axons

Early onset West syndrome with severe hypomyelination and coloboma‐like optic discs in a girl with SPTAN1 mutation

Immunological abnormalities in CHARGE syndrome

Red cell pyruvate kinase deficiency: 17 new mutations of the PK‐LR gene

De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise

Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome