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Results: 1-8 |
Results: 8
AXONAL NEUROPATHY AND PREDOMINANCE OF TYPE-II MYOFIBERS IN INFANTILE SPINAL MUSCULAR-ATROPHY
Authors: OMRAN H KETELSEN UP HEINEN F SAUER M RUDNIKSCHONEBORN S WIRTH B ZERRES K KRATZER W KORINTHENBERG R
Citation: H. Omran et al., AXONAL NEUROPATHY AND PREDOMINANCE OF TYPE-II MYOFIBERS IN INFANTILE SPINAL MUSCULAR-ATROPHY, Journal of child neurology, 13(7), 1998, pp. 327-331
DIAGNOSIS OF IDIOPATHIC MYOSITIS - VALUE OF (99M)TECHNETIUM PYROPHOSPHATE MUSCLE SCINTIGRAPHY AND MAGNETIC-RESONANCE-IMAGING IN TARGETED MUSCLE BIOPSY
Authors: VONKEMPIS J KALDEN P GUTFLEISCH J GRIMBACHER B KRAUSE T UHL M KETELSEN UP VOLK B ROTHER E VAITH P PETER HH
Citation: J. Vonkempis et al., DIAGNOSIS OF IDIOPATHIC MYOSITIS - VALUE OF (99M)TECHNETIUM PYROPHOSPHATE MUSCLE SCINTIGRAPHY AND MAGNETIC-RESONANCE-IMAGING IN TARGETED MUSCLE BIOPSY, Rheumatology international, 17(5), 1998, pp. 207-213
ABUNDANT MINUTE MYOTUBES IN A PATIENT WHO LATER DEVELOPED CENTRONUCLEAR MYOPATHY
Authors: WOCKEL L KETELSEN UP STOTTER M LAULE S MEYERMANN R BORNEMANN A
Citation: L. Wockel et al., ABUNDANT MINUTE MYOTUBES IN A PATIENT WHO LATER DEVELOPED CENTRONUCLEAR MYOPATHY, Acta Neuropathologica, 95(5), 1998, pp. 547-551
RARE COMBINATION OF BECKER-MUSCULAR-DYSTROPHY AND KLINEFELTERS-SYNDROME IN ONE PATIENT
Authors: ZEITOUN O KETELSEN UP WOLFF G MULLER CR KORINTHENBERG R
Citation: O. Zeitoun et al., RARE COMBINATION OF BECKER-MUSCULAR-DYSTROPHY AND KLINEFELTERS-SYNDROME IN ONE PATIENT, Brain & development, 19(5), 1997, pp. 359-361
CONGENITAL AXONAL NEUROPATHY CAUSED BY DELETIONS IN THE SPINAL MUSCULAR-ATROPHY REGION
Authors: KORINTHENBERG R SAUER M KETELSEN UP HANEMANN CO STOLL G GRAF M BABORIE A VOLK B WIRTH B RUDNIKSCHONEBORN S ZERRES K
Citation: R. Korinthenberg et al., CONGENITAL AXONAL NEUROPATHY CAUSED BY DELETIONS IN THE SPINAL MUSCULAR-ATROPHY REGION, Annals of neurology, 42(3), 1997, pp. 364-368
EOSINOPHILIC FASCIITIS (SHULMAN-SYNDROME)
Authors: SACH M BURGER JA ENGELHARDT A KETELSEN UP SCHOLLMEYER P
Citation: M. Sach et al., EOSINOPHILIC FASCIITIS (SHULMAN-SYNDROME), Der Internist, 38(7), 1997, pp. 688-691
3.1-KB DELETION OF MITOCHONDRIAL-DNA IN A PATIENT WITH KEARNS-SAYRE SYNDROME
Authors: KLOPSTOCK T BISCHOF F GEROK K DEUSCHL G SEIBEL P KETELSEN UP REICHMANN H
Citation: T. Klopstock et al., 3.1-KB DELETION OF MITOCHONDRIAL-DNA IN A PATIENT WITH KEARNS-SAYRE SYNDROME, Acta Neuropathologica, 90(2), 1995, pp. 126-129
RHABDOMYOLYSIS IN CARNITIN-PALMITOYL-TRAN SFERASE DEFICIENCY
Authors: REIFF A ZIMMERHACKL LB KETELSEN UP LEITITIS JU BRANDIS M REICHMANN H
Citation: A. Reiff et al., RHABDOMYOLYSIS IN CARNITIN-PALMITOYL-TRAN SFERASE DEFICIENCY, Monatsschrift fur Kinderheilkunde, 142(11), 1994, pp. 868-871
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