Nadine Kraemer

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Heba Gamal Farag, Sebastian Froehler, Konrad Oexle et al. · Orphanet Journal of Rare Diseases · 2013 · 44 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutations in <i>PTRH2</i> cause novel infantile‐onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness

Hao Hu, Michelle L. Matter, Lina Issa‐Jahns et al. · Annals of Clinical and Translational Neurology · 2014 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

CDK5RAP2 Expression During Murine and Human Brain Development Correlates with Pathology in Primary Autosomal Recessive Microcephaly

Lina Issa, Nadine Kraemer, Christian Rickert et al. · Cerebral Cortex · 2012 · 36 citations · Full text

Life Sciences, Developmental Biology, Neuroscience +17

Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation

Lina Issa, Katrin Mueller, Katja Seufert et al. · Orphanet Journal of Rare Diseases · 2013 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Effects of Helicobacter pylori on histamine and carbachol stimulated acid secretion by human parietal cells.

H Jablonowski, K. J. Hengels, Nadine Kraemer et al. · Gut · 1994 · 33 citations · Full text

Medicine, Microbiology, Pharmacology +17