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Results: 1-18 |
Results: 18
MITOCHONDRIAL-DNA HAPLOGROUP-U AS A RISK FACTOR FOR OCCIPITAL STROKE IN MIGRAINE
Authors: MAJAMAA K FINNILA S TURKKA J HASSINEN IE
Citation: K. Majamaa et al., MITOCHONDRIAL-DNA HAPLOGROUP-U AS A RISK FACTOR FOR OCCIPITAL STROKE IN MIGRAINE, Lancet, 352(9126), 1998, pp. 455-456
CLINICAL AND PHYSIOLOGICAL FINDINGS IN THE SKIN OF PATIENTS WITH THE COMMON MELAS MUTATION IN MITOCHONDRIAL-DNA
Authors: KARVONEN SL HAAPASAARI KM KALLIOINEN M OIKARINEN A HASSINEN IE MAJAMAA K
Citation: Sl. Karvonen et al., CLINICAL AND PHYSIOLOGICAL FINDINGS IN THE SKIN OF PATIENTS WITH THE COMMON MELAS MUTATION IN MITOCHONDRIAL-DNA, Journal of investigative dermatology, 110(4), 1998, pp. 572-572
EPIDEMIOLOGY OF A3243G, THE MUTATION FOR MITOCHONDRIAL ENCEPHALOMYOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES - PREVALENCE OF THE MUTATION IN AN ADULT-POPULATION
Authors: MAJAMAA K MOILANEN JS UIMONEN S REMES AM SALMELA PI KARPPA M MAJAMAAVOLTTI KAM RUSANEN H SORRI M PEUHKURINEN KJ HASSINEN IE
Citation: K. Majamaa et al., EPIDEMIOLOGY OF A3243G, THE MUTATION FOR MITOCHONDRIAL ENCEPHALOMYOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES - PREVALENCE OF THE MUTATION IN AN ADULT-POPULATION, American journal of human genetics, 63(2), 1998, pp. 447-454
METABOLIC INTERVENTIONS AGAINST COMPLEX-I DEFICIENCY IN MELAS SYNDROME
Authors: MAJAMAA K RUSANEN H REMES A HASSINEN IE
Citation: K. Majamaa et al., METABOLIC INTERVENTIONS AGAINST COMPLEX-I DEFICIENCY IN MELAS SYNDROME, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 291-296
THE COMMON MELAS MUTATION A3243G IN MITOCHONDRIAL-DNA AMONG YOUNG-PATIENTS WITH AN OCCIPITAL BRAIN INFARCT
Authors: MAJAMAA K TURKKA J KARPPA M WINQVIST S HASSINEN IE
Citation: K. Majamaa et al., THE COMMON MELAS MUTATION A3243G IN MITOCHONDRIAL-DNA AMONG YOUNG-PATIENTS WITH AN OCCIPITAL BRAIN INFARCT, Neurology, 49(5), 1997, pp. 1331-1334
ASSESSMENT OF INTRATHECAL COLLAGEN-SYNTHESIS BY ANALYSIS OF THE CEREBROSPINAL-FLUID
Authors: SAJANTI J MAJAMAA K
Citation: J. Sajanti et K. Majamaa, ASSESSMENT OF INTRATHECAL COLLAGEN-SYNTHESIS BY ANALYSIS OF THE CEREBROSPINAL-FLUID, Neurology, 48(3), 1997, pp. 4015-4015
PREVALENCE OF THE BASE-PAIR (BP) 3243-MUTATION IN MITOCHONDRIAL-DNA (MTDNA) IN YOUNG-PATIENTS WITH AN OCCIPITAL STROKE
Authors: MAJAMAA K TURKKA J KARPPA M WINQVIST S HASSINEN IE
Citation: K. Majamaa et al., PREVALENCE OF THE BASE-PAIR (BP) 3243-MUTATION IN MITOCHONDRIAL-DNA (MTDNA) IN YOUNG-PATIENTS WITH AN OCCIPITAL STROKE, Neurology, 48(3), 1997, pp. 6012-6012
POLYNEUROPATHY IN THE MTDNA BASE-PAIR-3243 POINT MUTATION - REPLY
Authors: MAJAMAA K TOLONEN U RUSANEN H REMES AM MYLLYLA R HASSINEN IE
Citation: K. Majamaa et al., POLYNEUROPATHY IN THE MTDNA BASE-PAIR-3243 POINT MUTATION - REPLY, Neurology, 46(5), 1996, pp. 1495-1496
INCREASE OF BLOOD NAD(+) AND ATTENUATION OF LACTACIDEMIA DURING NICOTINAMIDE TREATMENT OF A PATIENT WITH THE MELAS SYNDROME
Authors: MAJAMAA K RUSANEN H REMES AM PYHTINEN J HASSINEN IE
Citation: K. Majamaa et al., INCREASE OF BLOOD NAD(+) AND ATTENUATION OF LACTACIDEMIA DURING NICOTINAMIDE TREATMENT OF A PATIENT WITH THE MELAS SYNDROME, Life sciences, 58(8), 1996, pp. 691-699
INCREASED CONCENTRATIONS OF PROCOLLAGEN PROPEPTIDES IN THE CEREBROSPINAL-FLUID AFTER SUBARACHNOID HEMORRHAGE SUGGEST A MENINGEAL FIBROTIC REACTION
Authors: SAJANTI J HEIKKINEN E MAJAMAA K
Citation: J. Sajanti et al., INCREASED CONCENTRATIONS OF PROCOLLAGEN PROPEPTIDES IN THE CEREBROSPINAL-FLUID AFTER SUBARACHNOID HEMORRHAGE SUGGEST A MENINGEAL FIBROTIC REACTION, Annals of neurology, 38(2), 1995, pp. 319-319
DEMYELINATING POLYNEUROPATHY IN A PATIENT WITH THE TRNA(LEU(UUR)), MUTATION AT BASE-PAIR-3243 OF THE MITOCHONDRIAL-DNA
Authors: RUSANEN H MAJAMAA K TOLONEN U REMES AM MYLLYLA R HASSINEN IE
Citation: H. Rusanen et al., DEMYELINATING POLYNEUROPATHY IN A PATIENT WITH THE TRNA(LEU(UUR)), MUTATION AT BASE-PAIR-3243 OF THE MITOCHONDRIAL-DNA, Neurology, 45(6), 1995, pp. 1188-1192
FAMILIAL AGGREGATION OF CERVICAL ARTERY DISSECTION AND CEREBRAL ANEURYSM
Authors: MAJAMAA K PORTIMOJARVI H SOTANIEMI KA MYLLYLA VV
Citation: K. Majamaa et al., FAMILIAL AGGREGATION OF CERVICAL ARTERY DISSECTION AND CEREBRAL ANEURYSM, Stroke, 25(8), 1994, pp. 1704-1705
DEMYELINATING POLYNEUROPATHY IN A PATIENT WITH THE TRNA(LEU(UUR)) MTDNA MUTATION
Authors: MAJAMAA K RUSANEN H REMES A MYLLYLA R HASSINEN I
Citation: K. Majamaa et al., DEMYELINATING POLYNEUROPATHY IN A PATIENT WITH THE TRNA(LEU(UUR)) MTDNA MUTATION, Neurology, 44(4), 1994, pp. 10000285-10000285
A HERITABLE CONNECTIVE-TISSUE DISORDER IN PATIENTS WITH CAROTID-ARTERY DISSECTION
Authors: MAJAMAA K PORTIMOJARVI H TAIPALE L SOTANIEMI KA MYLLYLA VV
Citation: K. Majamaa et al., A HERITABLE CONNECTIVE-TISSUE DISORDER IN PATIENTS WITH CAROTID-ARTERY DISSECTION, Annals of neurology, 34(2), 1993, pp. 255-256
ADULT-ONSET DIABETES-MELLITUS AND NEUROSENSORY HEARING-LOSS IN MATERNAL RELATIVES OF MELAS PATIENTS IN A FAMILY WITH THE TRANSFER RNA(LEU)(UUR) MUTATION
Authors: REMES AM MAJAMAA K HERVA R HASSINEN IE
Citation: Am. Remes et al., ADULT-ONSET DIABETES-MELLITUS AND NEUROSENSORY HEARING-LOSS IN MATERNAL RELATIVES OF MELAS PATIENTS IN A FAMILY WITH THE TRANSFER RNA(LEU)(UUR) MUTATION, Neurology, 43(5), 1993, pp. 1015-1020
EXCLUSION OF MUTATIONS IN THE GENE FOR TYPE-III COLLAGEN (COL3A1) AS A COMMON-CAUSE OF INTRACRANIAL ANEURYSMS OR CERVICAL ARTERY DISSECTIONS - RESULTS FROM SEQUENCE-ANALYSIS OF THE CODING SEQUENCES OF TYPE-IIICOLLAGEN FROM 55 UNRELATED PATIENTS
Authors: KUIVANIEMI H PROCKOP DJ WU Y MADHATHERI SL KLEINERT C EARLEY JJ JOKINEN A STOLLE C MAJAMAA K MYLLYLA VV NORRGARD O SCHIEVINK WI MOKRI B FUKAWA O TERBERG JWM DEPAEPE A LOZANO AM LEBLANC R RYYNANEN M BAXTER BT SHIKATA H FERRELL RE TROMP G
Citation: H. Kuivaniemi et al., EXCLUSION OF MUTATIONS IN THE GENE FOR TYPE-III COLLAGEN (COL3A1) AS A COMMON-CAUSE OF INTRACRANIAL ANEURYSMS OR CERVICAL ARTERY DISSECTIONS - RESULTS FROM SEQUENCE-ANALYSIS OF THE CODING SEQUENCES OF TYPE-IIICOLLAGEN FROM 55 UNRELATED PATIENTS, Neurology, 43(12), 1993, pp. 2652-2658
SEQUENCING OF CDNA FROM 50 UNRELATED PATIENTS REVEALS THAT MUTATIONS IN THE TRIPLE-HELICAL DOMAIN OF TYPE-III PROCOLLAGEN ARE AN INFREQUENTCAUSE OF AORTIC-ANEURYSMS
Authors: TROMP G WU YL PROCKOP DJ MADHATHERI SL KLEINERT C EARLEY JJ ZHUANG JP NORRGARD O DARLING RC ABBOTT WM COLE CW JAAKKOLA P RYYNANEN M PEARCE WH YAO JST MAJAMAA K SMULLENS SN GATALICA Z FERRELL RE JIMENEZ SA JACKSON CE MICHELS VV KAYE M KUIVANIEMI H
Citation: G. Tromp et al., SEQUENCING OF CDNA FROM 50 UNRELATED PATIENTS REVEALS THAT MUTATIONS IN THE TRIPLE-HELICAL DOMAIN OF TYPE-III PROCOLLAGEN ARE AN INFREQUENTCAUSE OF AORTIC-ANEURYSMS, The Journal of clinical investigation, 91(6), 1993, pp. 2539-2545
A DISORDER OF COLLAGEN BIOSYNTHESIS IN PATIENTS WITH CEREBRAL-ARTERY ANEURYSM
Authors: MAJAMAA K MYLLYLA VV
Citation: K. Majamaa et Vv. Myllyla, A DISORDER OF COLLAGEN BIOSYNTHESIS IN PATIENTS WITH CEREBRAL-ARTERY ANEURYSM, Biochimica et biophysica acta, 1225(1), 1993, pp. 48-52
Risultati: 1-18 |