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Results: 1-25/37
Authors:
MULLERHOCKER J
JACOB U
SEIBEL P
Citation: J. Mullerhocker et al., THE COMMON 4977-BASE-PAIR DELETION OF MITOCHONDRIAL-DNA PREFERENTIALLY ACCUMULATES IN THE CARDIAC CONDUCTION SYSTEM OF PATIENTS WITH KEARNS-SAYRE-SYNDROME, Modern pathology, 11(3), 1998, pp. 295-301
Authors:
GRUNEWALD T
PORSCHKE H
GOEBEL H
REICHMANN H
SEIBEL P
Citation: T. Grunewald et al., CPEO WITH A NOVEL MTDNA DELETION AND A MUTATION IN THE TRNA(LEU(UUR))) GENE, Annals of neurology, 44(3), 1998, pp. 61-61
Authors:
MULLERHOCKER J
JACOB U
SEIBEL P
Citation: J. Mullerhocker et al., HASHIMOTO THYROIDITIS IS ASSOCIATED WITH DEFECTS OF CYTOCHROME-C-OXIDASE IN OXYPHIL ASKANAZY CELLS AND WITH THE COMMON DELETION (4,977) OF MITOCHONDRIAL-DNA, Ultrastructural pathology, 22(1), 1998, pp. 91-100
Authors:
DAMIAN MS
HERTEL A
SEIBEL P
REICHMANN H
BACHMANN G
SCHACHENMAYR W
HOER G
DORNDORF W
Citation: Ms. Damian et al., FOLLOW-UP IN CARRIERS OF THE MELAS MUTATION WITHOUT STROKES, European neurology, 39(1), 1998, pp. 9-15
Authors:
KLOPSTOCK T
NAUMANN M
SEIBEL P
SHALKE B
REINERS K
REICHMANN H
Citation: T. Klopstock et al., MITOCHONDRIAL-DNA MUTATIONS IN MULTIPLE SYMMETRICAL LIPOMATOSIS, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 271-275
Authors:
MULLERHOCKER J
AUST D
ROHRBACH H
NAPIWOTZKY J
REITH A
LINK TA
SEIBEL P
HOLZEL D
KADENBACH B
Citation: J. Mullerhocker et al., DEFECTS OF THE RESPIRATORY-CHAIN IN THE NORMAL HUMAN LIVER AND IN CIRRHOSIS DURING AGING, Hepatology, 26(3), 1997, pp. 709-719
Authors:
NAUMANN M
KIEFER R
TOYKA KV
SOMMER C
SEIBEL P
REICHMANN H
Citation: M. Naumann et al., MITOCHONDRIAL DYSFUNCTION WITH MYOCLONUS EPILEPSY AND RAGGED-RED FIBERS POINT MUTATION IN NERVE, MUSCLE, AND ADIPOSE-TISSUE OF A PATIENT WITH MULTIPLE SYMMETRICAL LIPOMATOSIS, Muscle & nerve, 20(7), 1997, pp. 833-839
Authors:
FLIERL A
REICHMANN H
SEIBEL P
Citation: A. Flierl et al., PATHOPHYSIOLOGY OF THE MELAS-3243 TRANSITION MUTATION, The Journal of biological chemistry, 272(43), 1997, pp. 27189-27196
Authors:
SCHOLS L
REICHMANN H
AMOIRIDIS G
SEIBEL P
WAGENER S
SEUFERT S
PRZUNTEK H
Citation: L. Schols et al., MITOCHONDRIAL DISORDERS IN DEGENERATIVE ATAXIAS, European journal of neurology, 3(1), 1996, pp. 55-60
Authors:
OEXLE K
OBERLE J
FINCKH B
KOHLSCHUTTER A
NAGY M
SEIBEL P
SEISSLER J
HUBNER C
Citation: K. Oexle et al., ISLET-CELL ANTIBODIES IRM DIABETES-MELLITUS ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE MUTATION, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 104(3), 1996, pp. 212-217
Authors:
SEIBEL P
GRUNEWALD T
GUNDOLLA A
DIENER HC
REICHMANN H
Citation: P. Seibel et al., INVESTIGATION ON THE MITOCHONDRIAL TRANSFER RNA(LEU(UUR)) IN BLOOD-CELLS FROM PATIENTS WITH CLUSTER HEADACHE, Journal of neurology, 243(4), 1996, pp. 305-307
Authors:
DAMIAN MS
SEIBEL P
SCHACHENMAYR W
REICHMANN H
DORNDORF W
Citation: Ms. Damian et al., VACTERL WITH THE MITOCHONDRIAL NP-3243 POINT MUTATION, American journal of medical genetics, 62(4), 1996, pp. 398-403
Authors:
MULLERHOCKER J
AUST D
NAPIWOTZKY J
MUNSCHER C
LINK TA
SEIBEL P
SCHNEEWEISS SG
KADENBACH B
Citation: J. Mullerhocker et al., DEFECTS OF THE RESPIRATORY-CHAIN IN OXYPHIL AND CHIEF CELLS OF THE NORMAL PARATHYROID AND IN HYPERFUNCTION, Human pathology, 27(6), 1996, pp. 532-541
Authors:
KLOPSTOCK T
MAY A
SEIBEL P
PAPAGIANNULI E
DIENER HC
REICHMANN H
Citation: T. Klopstock et al., MITOCHONDRIAL-DNA IN MIGRAINE WITH AURA, Neurology, 46(6), 1996, pp. 1735-1738
Authors:
KLOPSTOCK T
MAY A
SEIBEL P
PAPAGIANNULI E
DIENER HC
REICHMANN H
Citation: T. Klopstock et al., MITOCHONDRIAL-DNA IN MIGRAINE WITH AURA (VOL 46, PG 1735, 1996), Nervenarzt, 67(10), 1996, pp. 845-845
Authors:
GOLD R
SEIBEL P
REINELT G
SCHINDLER R
LANDWEHR P
BECK A
REICHMANN H
Citation: R. Gold et al., PHOSPHORUS MAGNETIC-RESONANCE SPECTROSCOPY IN THE EVALUATION OF MITOCHONDRIAL MYOPATHIES - RESULTS OF A 6-MONTH THERAPY STUDY WITH COENZYME-Q, European neurology, 36(4), 1996, pp. 191-196
Authors:
REICHMANN H
VOGLER L
SEIBEL P
Citation: H. Reichmann et al., RAGGED-RED OR RAGGED BLUE FIBERS, European neurology, 36(2), 1996, pp. 98-102
Authors:
SEIBEL P
TRAPPE J
Citation: P. Seibel et J. Trappe, A GENETIC THERAPY STRATEGY FOR THE TREATM ENT OF DISORDERS IN ENERGY-METABOLISM, Chemie in Unserer Zeit, 30(5), 1996, pp. 235-243
Authors:
REICHMANN H
SCHALKE B
SEIBEL P
NAUMANN M
TOYKA K
Citation: H. Reichmann et al., SARCOID MYOPATHY END MITOCHONDRIAL RESPIRATORY-CHAIN DEFECTS - CLINICOPATHOLOGICAL, BIOCHEMICAL AND MOLECULAR BIOLOGICAL ANALYSES, Neuromuscular disorders, 5(4), 1995, pp. 277-283
Authors:
DAMIAN M
SEIBEL P
REICHMANN H
SCHACHENMAYR W
DORNDORF W
Citation: M. Damian et al., PHENOTYPES OF THE MITOCHONDRIAL ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE MUTATION, Annals of neurology, 38(2), 1995, pp. 332-332
Authors:
BARBIROLI B
MEDORI R
TRITSCHLER HJ
KLOPSTOCK T
SEIBEL P
REICHMANN H
IOTTI S
LODI R
ZANIOL P
Citation: B. Barbiroli et al., LIPOIC (THIOCTIC) ACID INCREASES BRAIN ENERGY AVAILABILITY AND SKELETAL-MUSCLE PERFORMANCE AS SHOWN BY IN-VIVO P-31-MRS IN A PATIENT WITH MITOCHONDRIAL CYTOPATHY, Journal of neurology, 242(7), 1995, pp. 472-477
Authors:
SEIBEL P
TRAPPE J
VILLANI G
KLOPSTOCK T
PAPA S
REICHMANN H
Citation: P. Seibel et al., TRANSFECTION OF MITOCHONDRIA - STRATEGY TOWARDS A GENE-THERAPY OF MITOCHONDRIAL-DNA DISEASES, Nucleic acids research, 23(1), 1995, pp. 10-17
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
Authors:
DAMIAN MS
SEIBEL P
REICHMANN H
SCHACHENMAYR W
LAUBE H
BACHMANN G
WASSILL KH
DORNDORF W
Citation: Ms. Damian et al., CLINICAL SPECTRUM OF THE MELAS MUTATION IN A LARGE PEDIGREE, Acta neurologica Scandinavica, 92(5), 1995, pp. 409-415
Authors:
MELL OC
SEIBEL P
KADENBACH B
Citation: Oc. Mell et al., STRUCTURAL ORGANIZATION OF THE RAT GENES ENCODING LIVER-TYPE AND HEART-TYPE OF CYTOCHROME-C-OXIDASE SUBUNIT-VIA AND A PSEUDOGENE RELATED TOTHE COXVIA-L CDNA, Gene, 140(2), 1994, pp. 179-186