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Journal of Inherited Metabolic Disease|January 1, 1985
The role of vitamin E in the treatment of the neurological features of abetalipoproteinaemia and other disorders of fat absorptionD P Muller, J K Lloyd, O H WolffClinical Genetics|November 22, 2011
DFNB49 is an important cause of non-syndromic deafness in Czech Roma patients but not in the general Czech populationD Šafka Brožková, J Laštůvková, H Štěpánková, et al.Pharmaceutisch Weekblad. Scientific Edition|October 25, 1985
Synthesis and radioreceptor binding activity of N-0437, a new, extremely potent and selective D2 dopamine receptor agonistA S Horn, P Tepper, J Van der Weide, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 1, 1993
Schizophrenia: dopamine D1 receptor sequence is normal, but has DNA polymorphismsK Ohara, C Ulpian, P Seeman, et al.Molecular Pharmacology|July 1, 1988
Dopamine D1 receptors of the calf parathyroid gland: identification and characterizationH B Niznik, E L Fogel, C J Chen, et al.Journal of Psychiatry & Neuroscience : JPN|October 24, 1998
The human serotonin-7 receptor pseudogene: variation and chromosome locationD Nam, I H Qian, I Kusumi, et al.European Journal of Neurology|April 16, 2008
A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMTL Baránková, D Sisková, K Hühne, et al.Neuromuscular Disorders : NMD|October 4, 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosisE Mikesová, K Hühne, B Rautenstrauss, et al.Blut|January 1, 1982
Klinefelter's syndrome and acute non-lymphocytic leukemiaS J Muts-Homsma, H P Muller, J P GeraedstJournal of Vision|April 28, 2007
Living up to optimal expectationsC M P Muller, E Brenner, J B J SmeetsPageof 95