Authors:
DINKEL K
MEINCK HM
JURY KM
KARGES W
RICHTER W
Citation: K. Dinkel et al., INHIBITION OF GAMMA-AMINOBUTYRIC-ACID SYNTHESIS BY GLUTAMIC-ACID DECARBOXYLASE AUTOANTIBODIES IN STIFF-MAN SYNDROME, Annals of neurology, 44(2), 1998, pp. 194-201
Authors:
PIETZ J
DUNCKELMANN R
RUPP A
RATING D
MEINCK HM
SCHMIDT H
BREMER HJ
Citation: J. Pietz et al., NEUROLOGICAL OUTCOME IN ADULT PATIENTS WITH EARLY-TREATED PHENYLKETONURIA, European journal of pediatrics, 157(10), 1998, pp. 824-830
Authors:
WELLER E
BACHERT P
MEINCK HM
FRIEDMANN B
BARTSCH P
MAIRBAURL H
Citation: E. Weller et al., LACK OF EFFECT OF ORAL MG-SUPPLEMENTATION ON MG IN SERUM, BLOOD-CELLS, AND CALF MUSCLE, Medicine and science in sports and exercise, 30(11), 1998, pp. 1584-1591
Authors:
ROSIN L
DECAMILLI P
BUTLER M
SOLIMENA M
SCHMITT HP
MORGENTHALER N
MEINCK HM
Citation: L. Rosin et al., STIFF-MAN SYNDROME IN A WOMAN WITH BREAST-CANCER - AN UNCOMMON CENTRAL-NERVOUS-SYSTEM PARANEOPLASTIC-SYNDROME, Neurology, 50(1), 1998, pp. 94-98
Authors:
MORGENTHALER NG
SEISSLER J
ACHENBACH P
GLAWE D
PAYTON M
MEINCK HM
CHRISTIE MR
SCHERBAUM WA
Citation: Ng. Morgenthaler et al., ANTIBODIES TO THE TYROSINE PHOSPHATASE-LIKE PROTEIN IA-2 ARE HIGHLY ASSOCIATED WITH IDDM, BUT NOT WITH AUTOIMMUNE ENDOCRINE DISEASES OR STIFF MAN SYNDROME, Autoimmunity, 25(4), 1997, pp. 203-211
Citation: H. Steffen et al., IMMUNE-MEDIATED RETINOPATHY IN STIFF MAN SYNDROME, Investigative ophthalmology & visual science, 38(4), 1997, pp. 5231-5231
Authors:
STAYER C
TRONNIER V
DRESSNANDT J
MAUCH E
MARQUARDT G
RIEKE K
MULLERSCHWEFE G
SCHUMM F
MEINCK HM
Citation: C. Stayer et al., INTRATHECAL BACLOFEN THERAPY FOR STIFF-MAN SYNDROME AND PROGRESSIVE ENCEPHALOMYELOPATHY WITH RIGIDITY AND MYOCLONUS, Neurology, 49(6), 1997, pp. 1591-1597
Authors:
SPRANGER M
SCHWAB S
MEINCK HM
TISCHENDORF M
SIS J
BREITBART A
ANDRASSY K
Citation: M. Spranger et al., MENINGEAL INVOLVEMENT IN WEGENERS GRANULOMATOSIS CONFIRMED AND MONITORED BY POSITIVE CIRCULATING ANTINEUTROPHIL CYTOPLASM IN CEREBROSPINAL-FLUID, Neurology, 48(1), 1997, pp. 263-265
Authors:
HUND E
GRAU A
FOGEL W
FORSTING M
CANTZ M
KUSTERMANNKUHN B
HARZER K
NAVON R
GOEBEL HH
MEINCK HM
Citation: E. Hund et al., PROGRESSIVE CEREBELLAR-ATAXIA, PROXIMAL NEUROGENIC WEAKNESS AND OCULAR MOTOR DISTURBANCES - HEXOSAMINIDASE-A DEFICIENCY WITH LATE CLINICAL ONSET IN 4 SIBLINGS, Journal of the neurological sciences, 145(1), 1997, pp. 25-31
Authors:
SPRANGER M
SPRANGER S
TISCHENDORF M
MEINCK HM
CREMER M
Citation: M. Spranger et al., MYOTONIC-DYSTROPHY - THE ROLE OF LARGE TRIPLET REPEAT LENGTH IN THE DEVELOPMENT OF MENTAL-RETARDATION, Archives of neurology, 54(3), 1997, pp. 251-254
Citation: Ds. Tews et al., DNA-FRAGMENTATION AND APOPTOSIS-RELATED PROTEINS OF MUSCLE-CELLS IN MOTOR-NEURON DISORDERS, Acta neurologica Scandinavica, 96(6), 1997, pp. 380-386
Authors:
WILDERMUTH S
SPRANGER S
SPRANGER M
RAUE F
MEINCK HM
Citation: S. Wildermuth et al., KOBBERLING-DUNNIGAN SYNDROME - A RARE CAUSE OF GENERALIZED MUSCULAR HYPERTROPHY, Muscle & nerve, 19(7), 1996, pp. 843-847
Authors:
ROELCKE U
HORNSTEIN C
HUND E
SCHMITT HP
SIESS R
KALTENMAIER M
FASSLER J
MEINCK HM
Citation: U. Roelcke et al., SUNBATH POLYNEURITIS - SUBACUTE AXONAL NEUROPATHY IN PERAZINE-TREATEDPATIENTS AFTER INTENSE SUN EXPOSURE, Muscle & nerve, 19(4), 1996, pp. 438-441
Authors:
FORSTER C
BRANDT T
HUND E
MEINCK HM
VONKUMMER R
BREITBART A
WILDEMANN B
Citation: C. Forster et al., TRIGEMINAL SENSORY NEUROPATHY IN CONNECTIVE-TISSUE DISEASE - EVIDENCEFOR THE SITE OF THE LESION, Neurology, 46(1), 1996, pp. 270-271
Authors:
BECKER CM
MULHARDT C
SAUL B
BRUNE W
KLING C
MEINCK HM
Citation: Cm. Becker et al., INHIBITORY GLYCINE RECEPTORS AND THE MOLECULAR-BIOLOGY OF HYPERTONIC MOTOR DISORDERS, Journal of neurochemistry, 66, 1996, pp. 1-1
Citation: J. Spiegel et al., POLYGRAPHIC ANALYSIS OF TREMOR - THE IMPA CT OF DISPARITIES OF TREMORFREQUENCIES FOR THE PATHOPHYSIOLOGY AND DIFFERENTIAL-DIAGNOSIS OF TREMOR, EEG-EMG, 27(2), 1996, pp. 76-79
Authors:
SPRANGER M
SPRANGER S
ZIEGAN J
LOSSNER J
MEINCK HM
Citation: M. Spranger et al., 3 FAMILIAL CASES PRESENTING WITH AN IMMOBILE SPINE - RIGID SPINE OR EMERY-DREIFUSS SYNDROME, Clinical genetics, 50(4), 1996, pp. 229-231
Authors:
BRUNE W
WEBER RG
SAUL B
DOEBERITZ MV
GRONDGINSBACH C
KELLERMANN K
MEINCK HM
BECKER CM
Citation: W. Brune et al., A GLRA1 NULL MUTATION IN RECESSIVE HYPEREKPLEXIA CHALLENGES THE FUNCTIONAL-ROLE OF GLYCINE RECEPTORS, American journal of human genetics, 58(5), 1996, pp. 989-997