Heterozygous R1101K mutation of the <i>DCTN1</i> gene in a family with ALS and FTD

Christoph Münch, Angela Rosenbohm, Anne‐Dorte Sperfeld, +8

Annals of Neurology

Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel‐based morphometry of 3‐D MRI

Jan Kassubek, Alexander Unrath, Hans‐Jürgen Huppertz, +4

Amyotrophic Lateral Sclerosis

NeuropsychologyMotor Control DisordersWhite MatterBrain MappingBrain Lesion +22

Two German Kindreds With Familial Amyotrophic Lateral Sclerosis Due to TARDBP Mutations

Peter Kühnlein, Anne‐Dorte Sperfeld, Ben Vanmassenhove, +6

Archives of Neurology

Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approach

Ali Yılmaz, Hans‐Jürgen Gdynia, Hannibal Baccouche, +7

Journal of Cardiovascular Magnetic Resonance

Whole brain‐based analysis of regional white matter tract alterations in rare motor neuron diseases by diffusion tensor imaging

Alexander Unrath, Hans‐Peter Müller, Axel Riecker, +3

Human Brain Mapping

Comprehensive analysis of the mutation spectrum in 301 German ALS families

Kathrin Müller, Dávid Brenner, Patrick Weydt, +27

Journal of Neurology Neurosurgery & Psychiatry

Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue

Nicolai Treiber, Pallab Maity, Karmveer Singh, +25

Aging Cell

Histopathological analysis of skeletal muscle in patients with Parkinson's disease and ‘dropped head’/‘bent spine’ syndrome

Hans‐Jürgen Gdynia, Anne‐Dorte Sperfeld, Alexander Unrath, +4

Parkinsonism & Related Disorders

Motor DysfunctionSpinal Cord InjurySkeletal MuscleNeurological DisorderMedicine +10

Severe sensorimotor neuropathy after intake of highest dosages of vitamin B6

Hans‐Jürgen Gdynia, Timo D. Müller, Anne‐Dorte Sperfeld, +4

Neuromuscular Disorders

Spinal Cord InjuryDiabetic NeuropathyClinical NutritionNeuropathic PainSevere Sensorimotor Neuropathy +8

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

Rubén Fernández‐Santiago, S. Hoenig, Peter Lichtner, +12

Journal of Neurology