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Results: 1-25 | 26-36 |
Results: 26-36/36
DIFFERENTIAL-DIAGNOSIS IN SPINAL AND BULBAR MUSCULAR-ATROPHY CLINICALAND MOLECULAR ASPECTS
Authors: JOBSIS GJ LOUWERSE ES DEVISSER M WOLTERMAN RA BOLHUIS PA BUSCH HFM BRUGGENWIRTH HT BAAS F WIERSINGA WM KOELMAN JHTM DEJONG JMBV
Citation: Gj. Jobsis et al., DIFFERENTIAL-DIAGNOSIS IN SPINAL AND BULBAR MUSCULAR-ATROPHY CLINICALAND MOLECULAR ASPECTS, Journal of the neurological sciences, 129, 1995, pp. 56-57
GENETIC NONALLELIC HETEROGENITY CONFIRMED IN NEMALINE (ROD) MYOPATHY
Authors: WALLGRENPETERSSON C AVELA K MARCHAND S HANSEN FJ MUNTONI F DEVISSER M FAURE S DELACHAPELLE A
Citation: C. Wallgrenpetersson et al., GENETIC NONALLELIC HETEROGENITY CONFIRMED IN NEMALINE (ROD) MYOPATHY, American journal of human genetics, 57(4), 1995, pp. 1177-1177
DELETIONS OF THE SURVIVAL MOTOR-NEURON GENE IN UNAFFECTED SIBLINGS OFPATIENTS WITH SPINAL MUSCULAR-ATROPHY
Authors: COBBEN JM VANDERSTEEGE G GROOTSCHOLTEN P DEVISSER M SCHEFFER H BUYS CHCM
Citation: Jm. Cobben et al., DELETIONS OF THE SURVIVAL MOTOR-NEURON GENE IN UNAFFECTED SIBLINGS OFPATIENTS WITH SPINAL MUSCULAR-ATROPHY, American journal of human genetics, 57(4), 1995, pp. 805-808
MACRO EMG FOLLOW-UP-STUDY IN POSTPOLIOMYELITIS PATIENTS
Authors: IVANYI B DEVISSER BWO NELEMANS PJ DEVISSER M
Citation: B. Ivanyi et al., MACRO EMG FOLLOW-UP-STUDY IN POSTPOLIOMYELITIS PATIENTS, Journal of neurology, 242(1), 1994, pp. 37-40
LIMB-GIRDLE MUSCULAR-DYSTROPHY - REAPPRAISAL OF A REJECTED ENTITY
Authors: VANDERKOOI AJ DEVISSER M BARTH PG
Citation: Aj. Vanderkooi et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY - REAPPRAISAL OF A REJECTED ENTITY, Clinical neurology and neurosurgery, 96(3), 1994, pp. 209-218
HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I - CLINICAL AND NEUROGRAPHICAL FEATURES OF THE 17P DUPLICATION SUBTYPE
Authors: HOOGENDIJK JE DEVISSER M BOLHUIS PA HART AAM DEVISSER BWO
Citation: Je. Hoogendijk et al., HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I - CLINICAL AND NEUROGRAPHICAL FEATURES OF THE 17P DUPLICATION SUBTYPE, Muscle & nerve, 17(1), 1994, pp. 85-90
APPARENT SMA-I UNLINKED TO 5Q
Authors: COBBEN JM SCHEFFER H DEVISSER M BEGEER JH MOLENAAR WM VANDERSTEEGE G BUYS CHCM VANOMMEN GJ TENKATE LP
Citation: Jm. Cobben et al., APPARENT SMA-I UNLINKED TO 5Q, Journal of Medical Genetics, 31(3), 1994, pp. 242-244
DELETION OF THE SERINE-34 CODON FROM THE MAJOR PERIPHERAL MYELIN PROTEIN-P(0) GENE IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1B
Authors: KULKENS T BOLHUIS PA WOLTERMAN RA KEMP S TENIJENHUIS S VALENTIJN LJ HENSELS GW JENNEKENS FGI DEVISSER M HOOGENDIJK JE BAAS F
Citation: T. Kulkens et al., DELETION OF THE SERINE-34 CODON FROM THE MAJOR PERIPHERAL MYELIN PROTEIN-P(0) GENE IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1B, Nature genetics, 5(1), 1993, pp. 35-39
ALTERNATIVELY SIZED DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A
Authors: VALENTIJN LJ BAAS F ZORN I HENSELS GW DEVISSER M BOLHUIS PA
Citation: Lj. Valentijn et al., ALTERNATIVELY SIZED DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A, Human molecular genetics, 2(12), 1993, pp. 2143-2146
POLIOVIRUS PERSISTENCE IN THE POSTPOLIO SYNDROME - REPLY
Authors: MELCHERS W DEVISSER M JONGEN P VANLOON A NIBBELING R OOSTVOGEL P WILLEMSE D GALAMA J
Citation: W. Melchers et al., POLIOVIRUS PERSISTENCE IN THE POSTPOLIO SYNDROME - REPLY, Annals of neurology, 34(3), 1993, pp. 416-417
ALLELIC HETEROGENEITY IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA (CHARCOT-MARIE-TOOTH DISEASE TYPE-1A)
Authors: HOOGENDIJK JE JANSSEN EAM GABREELSFESTEN AAWM HENSELS GW JOOSTEN EMG GABREELS FJM ZORN I VALENTIJN LJ BAAS F DEVISSER BWO DEVISSER M BOLHUIS PA
Citation: Je. Hoogendijk et al., ALLELIC HETEROGENEITY IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA (CHARCOT-MARIE-TOOTH DISEASE TYPE-1A), Neurology, 43(5), 1993, pp. 1010-1015
Risultati: 1-25 | 26-36 |