AAAAAA

   
Results: 1-9 |
Results: 9
FASCIAL TC-99M MDP UPTAKE IN EOSINOPHILIC FASCIITIS AS DEMONSTRATED BY SPECT
Authors: FLAMEN P DIERICKX L EVERAERT H REYCHLER R BRUYLAND M FRANKEN PR BOSSUYT A
Citation: P. Flamen et al., FASCIAL TC-99M MDP UPTAKE IN EOSINOPHILIC FASCIITIS AS DEMONSTRATED BY SPECT, Clinical nuclear medicine, 22(12), 1997, pp. 844-846
POLYMYOSITIS AS FIRST MANIFESTATION OF AUTOIMMUNE DISORDERS
Authors: BISSAY V MICHOTTE A SCHMEDDING E BRUYLAND M VERVAECK M FLAMEZ A EBINGER G
Citation: V. Bissay et al., POLYMYOSITIS AS FIRST MANIFESTATION OF AUTOIMMUNE DISORDERS, Acta neurologica belgica, 97(1), 1997, pp. 63-63
MOLECULAR-GENETIC ANALYSIS OF FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASELINKED TO CHROMOSOME 14Q24.3
Authors: CRUTS M BACKHOVENS H WANG SY VANGASSEN G THEUNS J DEJONGHE C WEHNERT A DEVOECHT J DEWINTER G CRAS P BRUYLAND M DATSON N WEISSENBACH J DENDUNNEN JT MARTIN JJ HENDRIKS L VANBROECKHOVEN C
Citation: M. Cruts et al., MOLECULAR-GENETIC ANALYSIS OF FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASELINKED TO CHROMOSOME 14Q24.3, Human molecular genetics, 4(12), 1995, pp. 2363-2371
BILATERAL STRIATAL NECROSIS WITH A NOVEL POINT MUTATION IN THE MITOCHONDRIAL ATPASE-6 GENE
Authors: DEMEIRLEIR L SENECA S LISSENS W SCHOENTJES E BRUYLAND M DESPRECHINS B LIEBAERS I
Citation: L. Demeirleir et al., BILATERAL STRIATAL NECROSIS WITH A NOVEL POINT MUTATION IN THE MITOCHONDRIAL ATPASE-6 GENE, Annals of neurology, 36(3), 1994, pp. 522-522
BENEFICIAL EFFECT OF A TREATMENT WITH XYLITOL IN A PATIENT WITH MYOADENYLATE DEAMINASE DEFICIENCY
Authors: BRUYLAND M EBINGER G
Citation: M. Bruyland et G. Ebinger, BENEFICIAL EFFECT OF A TREATMENT WITH XYLITOL IN A PATIENT WITH MYOADENYLATE DEAMINASE DEFICIENCY, Clinical neuropharmacology, 17(5), 1994, pp. 492-493
VIGABATRIN IN UNCONTROLLED SEIZURES - BELGIAN CLINICAL-EXPERIENCE
Authors: ALLEWAERT M LHOIR A BEUSEN L BOON P BRUYLAND M DEKEYSER J DEKLIPPEL N DEROUAUX M DEWIT P DHAENE T DHOOGHE M EYSKENS F FOSSELLE E GEENS K GODFROI M GOETHALS J GUILLAUME D JAEKEN J KULAKOWSKI S LALOUX P LEGRAND B LOWENTHAL A MAERE P MEERSMAN G MOL L MONSEU G PEETERS E PILLEN E PINTELON R RAETS Y ROOSE H ROOSE K SCALAIS E SZLIWOWSKI H TUGENDHAFT P VANCALSTER L VANDENBORRE R VANHAVER H VANZANDIJCKE M VINKEN L
Citation: M. Allewaert et al., VIGABATRIN IN UNCONTROLLED SEIZURES - BELGIAN CLINICAL-EXPERIENCE, Clinical neurology and neurosurgery, 96(1), 1994, pp. 42-46
HYPO-IGG IN MYOTONIC-DYSTROPHY IS DUE TO A SELECTIVE REDUCTION OF THEIGG1-SUBCLASS SERUM LEVEL
Authors: BRUYLAND M LISSENS W DEWAELE M DEMANET C
Citation: M. Bruyland et al., HYPO-IGG IN MYOTONIC-DYSTROPHY IS DUE TO A SELECTIVE REDUCTION OF THEIGG1-SUBCLASS SERUM LEVEL, Muscle & nerve, 17(10), 1994, pp. 1233-1234
DYNAMIC TRAINING OF SKELETAL-MUSCLE VENTRICLES - A METHOD TO INCREASEMUSCULAR POWER FOR CARDIAC ASSISTANCE
Authors: GULDNER NW EICHSTAEDT HC KLAPPROTH P TILMANS MHI THUAUDET S UMBRAIN V RUCK K WYFFELS E BRUYLAND M SIGMUND M MESSMER BJ BARDOS P
Citation: Nw. Guldner et al., DYNAMIC TRAINING OF SKELETAL-MUSCLE VENTRICLES - A METHOD TO INCREASEMUSCULAR POWER FOR CARDIAC ASSISTANCE, Circulation, 89(3), 1994, pp. 1032-1040
2 NOVEL MUTATIONS OF THE PORPHOBILINOGEN DEAMINASE GENE IN ACUTE INTERMITTENT PORPHYRIA
Authors: GU XF DEROOIJ F DEBAAR E BRUYLAND M LISSENS W NORDMANN Y GRANDCHAMP B
Citation: Xf. Gu et al., 2 NOVEL MUTATIONS OF THE PORPHOBILINOGEN DEAMINASE GENE IN ACUTE INTERMITTENT PORPHYRIA, Human molecular genetics, 2(10), 1993, pp. 1735-1736
Risultati: 1-9 |