Katja Grohmann

Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Katja Grohmann, Markus Schuelke, Alexander Diers et al. · Nature Genetics · 2001 · 341 citations

Transcriptional Regulation, Immunogenetics, Autoimmune Disease +8

Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Katja Grohmann, Raymonda Varon, Piroschka Stolz et al. · Annals of Neurology · 2003 · 171 citations

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Katja Grohmann · Human Molecular Genetics · 2004 · 92 citations · Full text

Long-Term Observations of Patients with Infantile Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)

Sabine Rudnik‐Schöneborn, Piroschka Stolz, Raymonda Varon et al. · Neuropediatrics · 2004 · 69 citations

Triple Knock-Out of<i>CNTF</i>,<i>LIF</i>, and<i>CT-1</i>Defines Cooperative and Distinct Roles of these Neurotrophic Factors for Motoneuron Maintenance and Function

Bettina Holtmann, Stefan Wiese, Mohtashem Samsam et al. · Journal of Neuroscience · 2005 · 66 citations · Full text