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Results: 1-25 | 26-26

Results: 1-25/26

SARCOGLYCAN DEFICIENCY CAUSES MUSCULAR-DYSTROPHY BY DISRUPTING THE ACTIN-BINDING FUNCTION OF DYSTROPHIN

Authors: KYRIAKIDES T MARQUEZ B CHRISTODOULOU K PANOUSOPOULOS A MIDDLETON LT

Citation: T. Kyriakides et al., SARCOGLYCAN DEFICIENCY CAUSES MUSCULAR-DYSTROPHY BY DISRUPTING THE ACTIN-BINDING FUNCTION OF DYSTROPHIN, Annals of neurology, 44(3), 1998, pp. 82-82

CLINICAL AND GENETIC-STUDIES OF A NOVEL FORM OF AUTOSOMAL RECESSIVE HEREDITARY MOTOR NEURONOPATHY

Authors: MIDDLETON LT ALQUDAH A ZAMBA E TSINGIS M HORAMI K MUBAIDIN A ABUSHEIK S ELKHATEEB M KYRIACOU K KYRIAKIDES T CHRISTODOULOU K

Citation: Lt. Middleton et al., CLINICAL AND GENETIC-STUDIES OF A NOVEL FORM OF AUTOSOMAL RECESSIVE HEREDITARY MOTOR NEURONOPATHY, Annals of neurology, 44(3), 1998, pp. 198-198

MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY

Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT

Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY, Human molecular genetics, 6(4), 1997, pp. 635-640

MOLECULAR-GENETICS OF AUTOSOMAL RECESSIVE HEREDITARY INCLUSION-BODY MYOPATHY

Authors: MIDDLETON LT CHRISTODOULOU K ASKANAS V ENGEL WK MCFERRIN J KYRIAKIDES T ZAMBA E PAPADOPOULLOU E

Citation: Lt. Middleton et al., MOLECULAR-GENETICS OF AUTOSOMAL RECESSIVE HEREDITARY INCLUSION-BODY MYOPATHY, Annals of neurology, 42(3), 1997, pp. 86-86

MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P

Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT

Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P, Neurology, 48(6), 1997, pp. 3-3

CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES

Authors: MIDDLETON LT CHRISTODOULOU K

Citation: Lt. Middleton et K. Christodoulou, CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES, Neurology, 48(3), 1997, pp. 3080-3080

DUCHENNE MUSCULAR-DYSTROPHY - WHEN TO COMMENCE STEROIDS

Authors: KYRIAKIDES T KYRIAKOU K SOEDIONO O MIDDLETON LT

Citation: T. Kyriakides et al., DUCHENNE MUSCULAR-DYSTROPHY - WHEN TO COMMENCE STEROIDS, Neurology, 48(3), 1997, pp. 3134-3134

GENETIC-HETEROGENEITY IN FRIEDREICHS-ATAXIA - INDICATION FOR A 2ND LOCUS ON CHROMOSOME-9

Authors: CHRISTODOULOU K DEYMEER F SERDAROGLU P OZDEMIR C GEORGIOU DM PAPADOPOULOU E ZAMBA E MIDDLETON LT

Citation: K. Christodoulou et al., GENETIC-HETEROGENEITY IN FRIEDREICHS-ATAXIA - INDICATION FOR A 2ND LOCUS ON CHROMOSOME-9, American journal of human genetics, 61(4), 1997, pp. 1579-1579

CMT2 MAPPING PROGRESS - CONFIRMATION OF A 2ND LOCUS AND EVIDENCE FOR ADDITIONAL GENETIC-HETEROGENEITY

Authors: LENNON F PERICAKVANCE MA SPEER MC WEST SG MENOLD MM STAJICH JM WOLPERT CM SLOTTERBECK BD SAITO M TIM RW ROZEAR MP MIDDLETON LT TSUJI S VANCE JM

Citation: F. Lennon et al., CMT2 MAPPING PROGRESS - CONFIRMATION OF A 2ND LOCUS AND EVIDENCE FOR ADDITIONAL GENETIC-HETEROGENEITY, American journal of human genetics, 61(4), 1997, pp. 1645-1645

MUTATION SCREENING IN THE SYNAPTOBREVIN-2 GENE IN PATIENTS WITH FAMILIAL INFANTILE MYASTHENIA

Authors: NEOCLEOUS V MIDDLETON LT CHRISTODOULOU K

Citation: V. Neocleous et al., MUTATION SCREENING IN THE SYNAPTOBREVIN-2 GENE IN PATIENTS WITH FAMILIAL INFANTILE MYASTHENIA, American journal of human genetics, 61(4), 1997, pp. 1997-1997

CONGENITAL MYASTHENIC SYNDROMES - 34TH ENMC INTERNATIONAL WORKSHOP, 10-11 JUNE 1995

Authors: MIDDLETON LT

Citation: Lt. Middleton, CONGENITAL MYASTHENIC SYNDROMES - 34TH ENMC INTERNATIONAL WORKSHOP, 10-11 JUNE 1995, Neuromuscular disorders, 6(2), 1996, pp. 133-136

EVIDENCE OF GENETIC-HETEROGENEITY WITHIN THE FRIEDREICHS ATAXIA PHENOTYPE

Authors: CHRISTODOULOU K OZCELIK T GEORGIOU DM PODA M SERDAROGLU P DEYMEER F OZDEMIR C IOANNOU P MIDDLETON LT

Citation: K. Christodoulou et al., EVIDENCE OF GENETIC-HETEROGENEITY WITHIN THE FRIEDREICHS ATAXIA PHENOTYPE, Annals of neurology, 40(3), 1996, pp. 226-226

CLINICAL AND MOLECULAR-GENETIC INVESTIGATION OF AN ATYPICAL FRIEDREICHS ATAXIA FAMILY

Authors: CHRISTODOULOU K OZCELIK T NICOSIA DMG PODA M SERDAROGLU P DEYMEER F OZDEMIR C IOANNOU P MIDDLETON LT

Citation: K. Christodoulou et al., CLINICAL AND MOLECULAR-GENETIC INVESTIGATION OF AN ATYPICAL FRIEDREICHS ATAXIA FAMILY, Neurology, 46(2), 1996, pp. 2103-2103

FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES

Authors: KYRIALLIS K CHRISTODOULOU K ALSHEHAB A BARBA V MYLONAS Y MAVROMATIS J SERDAROGLU P OZCELIK T DEYMMER F OZDEMIR C MIDDLETON LT

Citation: K. Kyriallis et al., FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES, Neurology, 46(2), 1996, pp. 4089-4089

MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P

Authors: CHRISTODOULOU K KYRIAKIDES T HRISTOVA AH GEORGIOU DM KALAYDJIEVA L YSHPEKOVA B IVANOVA T WEBER JL MIDDLETON LT

Citation: K. Christodoulou et al., MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P, Human molecular genetics, 4(9), 1995, pp. 1629-1632

CONSENSUS STATEMENT ON THE MANAGEMENT OF PATIENTS WITH ASYMPTOMATIC ATHEROSCLEROTIC CAROTID BIFURCATION LESIONS

Authors: NICOLAIDES AN BARNETT HJM BELCARO GV BERNSTEIN EF CALLOW A EASTCOTT HHG EIKELBOOM B EKLOF B GEROULAKOS G HALLIDAY A HOBSON R KALODIKI E LUSBY R MALIKIDES A MIDDLETON LT MOORE WS NORRIS J PRESCOTT L RAMASWAMI G RUTHERFORD R SANDMANN W SHANIK G SPARTERA C THOMAS D

Citation: An. Nicolaides et al., CONSENSUS STATEMENT ON THE MANAGEMENT OF PATIENTS WITH ASYMPTOMATIC ATHEROSCLEROTIC CAROTID BIFURCATION LESIONS, International angiology, 14(1), 1995, pp. 5-17

EFFICIENT TRAINING OF NEURAL-NETWORK MODELS IN CLASSIFICATION OF ELECTROMYOGRAPHIC DATA

Authors: PATTICHIS CS CHARALAMBOUS C MIDDLETON LT

Citation: Cs. Pattichis et al., EFFICIENT TRAINING OF NEURAL-NETWORK MODELS IN CLASSIFICATION OF ELECTROMYOGRAPHIC DATA, Medical & biological engineering & computing, 33(3), 1995, pp. 499-503

LINKAGE DISEQUILIBRIUM IN THE DUCHENNE-LIKE MUSCULAR-DYSTROPHY NDLMD)REGION REFINES THE LOCALIZATION OF THE DISEASE GENE TO LESS-THAN U CM

Authors: BENOTHMANE K SPEER M MIDDLETON LT LOEB D HENTATI F BENHAMIDA M PERICAKVANCE MA VANCE JM

Citation: K. Benothmane et al., LINKAGE DISEQUILIBRIUM IN THE DUCHENNE-LIKE MUSCULAR-DYSTROPHY NDLMD)REGION REFINES THE LOCALIZATION OF THE DISEASE GENE TO LESS-THAN U CM, Neurology, 45(4), 1995, pp. 243-243

WHAT IS THE REAL EPIDEMIOLOGY OF MYASTHENIA-GRAVIS

Authors: KYRIALLIS K HRISTOVA AH MIDDLETON LT

Citation: K. Kyriallis et al., WHAT IS THE REAL EPIDEMIOLOGY OF MYASTHENIA-GRAVIS, Neurology, 45(4), 1995, pp. 351-352

AUTOSOMAL-DOMINANT MOTOR NEURONOPATHY PREDOMINANTLY AFFECTING THE HANDS

Authors: MIDDLETON LT HRISTOVA AH KALAYDJIEVA L YSHPEKOVA B IVANOVA T CHRISTODOULOU K KYRIAKIDES T

Citation: Lt. Middleton et al., AUTOSOMAL-DOMINANT MOTOR NEURONOPATHY PREDOMINANTLY AFFECTING THE HANDS, Neurology, 45(4), 1995, pp. 448-448

NEURAL-NETWORK MODELS IN EMG DIAGNOSIS

Authors: PATTICHIS CS SCHIZAS CN MIDDLETON LT

Citation: Cs. Pattichis et al., NEURAL-NETWORK MODELS IN EMG DIAGNOSIS, IEEE transactions on biomedical engineering, 42(5), 1995, pp. 486-496

MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P

Authors: CHRISTODOULOU K KYRIAKIDES T HRISTOVA AH GEORGIOU DM KALAJDJIEVA L YSHPEKOVA B IVANOVA T WEBER JL MIDDLETON LT

Citation: K. Christodoulou et al., MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P, American journal of human genetics, 57(4), 1995, pp. 1082-1082

23RD ENMC WORKSHOP ON RARE NEUROMUSCULAR DISEASES - 4-6 JUNE, BAARN, THE NETHERLANDS

Authors: MIDDLETON LT MOSER H

Citation: Lt. Middleton et H. Moser, 23RD ENMC WORKSHOP ON RARE NEUROMUSCULAR DISEASES - 4-6 JUNE, BAARN, THE NETHERLANDS, Neuromuscular disorders, 4(3), 1994, pp. 273-275

NOVEL CYSTIC-FIBROSIS MUTATION ASSOCIATED WITH MILD DISEASE IN CYPRIOT PATIENTS

Authors: BOTEVA K PAPAGEORGIOU E GEORGIOU C ANGASTINIOTIS M MIDDLETON LT CONSTANTINOUDELTAS CD

Citation: K. Boteva et al., NOVEL CYSTIC-FIBROSIS MUTATION ASSOCIATED WITH MILD DISEASE IN CYPRIOT PATIENTS, Human genetics, 93(5), 1994, pp. 529-532

LOCALIZATION OF A GENE (CMT2A) FOR AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 TO CHROMOSOME-1P AND EVIDENCE OF GENETIC-HETEROGENEITY

Authors: BENOTHMANE K MIDDLETON LT LOPREST LJ WILKINSON KM LENNON F ROZEAR MP STAJICH JM GASKELL PC ROSES AD PERICAKVANCE MA VANCE JM

Citation: K. Benothmane et al., LOCALIZATION OF A GENE (CMT2A) FOR AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 TO CHROMOSOME-1P AND EVIDENCE OF GENETIC-HETEROGENEITY, Genomics, 17(2), 1993, pp. 370-375

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