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    1. Street, VA; Goldy, JD; Golden, AS; Tempel, BL; Bird, TD; Chance, PF
      Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Finsterer, J; Lubec, D; Samec, P
      Generalised spinal cord atrophy, Chiari-I malformation, and syringomyelia

      SPINAL CORD
    3. Huang, JH; Soliman, I
      Anaesthetic management for a patient with Dejerine-Sottas disease and asthma

      PAEDIATRIC ANAESTHESIA
    4. Date, H; Onodera, O; Tanaka, H; Iwabuchi, K; Uekawa, K; Igarashi, S; Koike, R; Hiroi, T; Yuasa, T; Awaya, Y; Sakai, T; Takahashi, T; Nagatomo, H; Sekijima, Y; Kawachi, I; Takiyama, Y; Nishizawa, M; Fukuhara, N; Saito, K; Sugano, S; Tsuji, S
      Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is causedby mutations in a new HIT superfamily gene

      NATURE GENETICS
    5. Moreira, MC; Barbot, C; Tachi, N; Kozuka, N; Uchida, E; Gibson, T; Mendonca, P; Costa, M; Barros, J; Yanagisawa, T; Watanabe, M; Ikeda, Y; Aoki, M; Nagata, T; Coutinho, P; Sequeiros, J; Koenig, M
      The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

      NATURE GENETICS
    6. Mostacciuolo, ML; Righetti, E; Zortea, M; Bosello, V; Schiavon, F; Vallo, L; Merlini, L; Siciliano, G; Fabrizi, GM; Rizzuto, N; Milani, M; Baratta, S; Taroni, F
      Charcot-Marie-Tooth disease type I and related demyelinating neuropathies:Mutation analysis in a large cohort of Italian families

      HUMAN MUTATION
    7. Maurer, M; Schmid, CD; Bootz, F; Zielasek, J; Toyka, KV; Oehen, S; Martini, R
      Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants

      MOLECULAR AND CELLULAR NEUROSCIENCE
    8. Guilbot, A; Williams, A; Ravise, N; Verny, C; Brice, A; Sherman, DL; Brophy, PJ; LeGuern, E; Delague, V; Bareil, C; Megarbane, A; Claustres, M
      A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

      HUMAN MOLECULAR GENETICS
    9. Dubourg, O; Tardieu, S; Birouk, N; Gouider, R; Leger, JM; Maisonobe, T; Brice, A; Bouche, P; LeGuern, E
      The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity

      NEUROMUSCULAR DISORDERS
    10. Mohan, U; Misra, VP; Britto, J; Muntoni, F; King, RHM; Thomas, PK
      Inherited early onset severe axonal polyneuropathy with respiratory failure and autonomic involvement

      NEUROMUSCULAR DISORDERS
    11. Barhoumi, C; Amouri, R; Ben Hamida, C; Ben Hamida, M; Machghoul, S; Gueddiche, M; Hentati, F
      Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3

      NEUROMUSCULAR DISORDERS
    12. Norreel, JC; Jamon, M; Riviere, G; Passage, E; Fontes, M; Clarac, F
      Behavioural profiling of a murine Charcot-Marie-Tooth disease type 1A model

      EUROPEAN JOURNAL OF NEUROSCIENCE
    13. Zhou, RH; Kokame, K; Tsukamoto, Y; Yutani, C; Kato, H; Miyata, T
      Characterization of the human NDRG gene family: A newly identified member,NDRG4, is specifically expressed in brain and heart

      GENOMICS
    14. Lacy, PD; Hartley, BE; Rutter, MJ; Cotton, RT
      Familial bilateral vocal cord paralysis and Charcot-Marie-Tooth disease type II-C

      ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
    15. Nakai, Y; Okumura, A; Takada, H; Negoro, T; Watanabe, K; Hattori, N; Sobue, G
      Inflammatory pathological changes in a 2-year-old boy with Charcot-Marie-Tooth disease

      BRAIN & DEVELOPMENT
    16. Plante-Bordeneuve, V; Parman, Y; Guiochon-Mantel, A; Alj, Y; Deymeer, F; Serdaroglu, P; Eraksoy, M; Said, G
      The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases

      JOURNAL OF NEUROLOGY
    17. Yener, GG; Guiochon-Mantel, A; Obuz, F; Baklan, B; Ozturk, V; Kovanhkaya, I; Cakmur, R; Genc, A
      Phe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings

      JOURNAL OF NEUROLOGY
    18. Bodily, KD; Morrison, CM; Renden, RB; Broadie, K
      A novel member of the Ig superfamily, turtle, is a CNS-specific protein required for coordinated motor control

      JOURNAL OF NEUROSCIENCE
    19. Bergmann, C; Schroder, JM; Rudnik-Schneborn, S; Zerres, K; Senderek, J
      A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany

      MOLECULAR BRAIN RESEARCH
    20. Young, P; Suter, U
      Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease

      BRAIN RESEARCH REVIEWS
    21. Wilmshurst, JM; Bye, A; Rittey, C; Adams, C; Hahn, AF; Ramsay, D; Pamphlett, R; Pollard, JD; Ouvrier, R
      Severe infantile axonal neuropathy with respiratory failure

      MUSCLE & NERVE
    22. Dematteis, M; Pepin, JL; Jeanmart, M; Deschaux, C; Labarre-Vila, A; Levy, P
      Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study

      LANCET
    23. Fabrizi, GM; Ferrarini, M; Cavallaro, T; Jarre, L; Polo, A; Rizzuto, N
      A somatic and germline mosaic mutation in MPZ/P-0 mimics recessive inheritance of CMT1B

      NEUROLOGY
    24. Novak, V; Freimer, ML; Kissel, JT; Sahenk, Z; Periquet, IM; Nash, SM; Collins, MP; Mendell, JR
      Autonomic impairment in painful neuropathy

      NEUROLOGY
    25. Senderek, J; Ramaekers, VT; Zerres, K; Rudnik-Schoneborn, S; Schroder, JM; Bergmann, C
      Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    26. Gemignani, F; Marbini, A
      Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    27. Nakagawa, M; Matsuzaki, T; Suehara, M; Kanzato, N; Takashima, H; Higuchi, I; Matsumura, T; Goto, K; Arahata, K; Osame, M
      Phenotypic variation in a large Japanese family with Miyoshi myopathy withnonsense mutation in exon 19 of dysferlin gene

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    28. Carenini, S; Maurer, M; Werner, A; Blazyca, H; Toyka, KV; Schmid, CD; Raivich, G; Martini, R
      The role of macrophages in demyelinating peripheral nervous system of miceheterozygously deficient in P0

      JOURNAL OF CELL BIOLOGY
    29. Naumann, R; Mohm, J; Reuner, U; Kroschinsky, F; Rautenstrauss, B; Ehninger, G
      Early recognition of hereditary motor and sensory neuropathy type 1 can avoid life-threatening vincristine neurotoxicity

      BRITISH JOURNAL OF HAEMATOLOGY
    30. Hisama, FM; Lee, HH; Vashlishan, A; Tehumalla, P; Russell, DS; Auld, E; Goldstein, JM
      Clinical and molecular studies in a family with probable X-linked dominantCharcot-Marie-Tooth disease involving the central nervous system

      ARCHIVES OF NEUROLOGY
    31. Ginz, HF; Ummenhofer, WC; Erb, T; Urwyler, A
      The hereditary motor-sensory neuropathy Charcot-Marie-Tooth disease: a case report and a review of the literature

      ANAESTHESIST
    32. Kennerson, ML; Zhu, D; Gardner, RJM; Storey, E; Merory, J; Robertson, SP; Nicholson, GA
      Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. Verhoeven, K; Villanova, M; Rossi, A; Malandrini, A; De Jonghe, P; Timmerman, V
      Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1

      AMERICAN JOURNAL OF HUMAN GENETICS
    34. Moreira, MD; Barbot, C; Tachi, N; Kozuka, N; Mendonca, P; Barros, J; Coutinho, P; Sequeiros, J; Koenig, M
      Homozygosity mapping of portuguese and Japanese forms of ataxia-oculomotorapraxia to 9p13, and evidence for genetic heterogeneity

      AMERICAN JOURNAL OF HUMAN GENETICS
    35. Hahn, AF; Ainsworth, PJ; Bolton, CF; Bilbao, JM; Vallat, JM
      Pathological findings in the x-linked form of Charcot-Marie-Tooth disease:a morphometric and ultrastructural analysis

      ACTA NEUROPATHOLOGICA
    36. Cruz-Martinez, A; Armijo, A; Fermoso, A; Moraleda, S; Mate, I; Marin, M
      Phrenic nerve conduction study in demyelinating neuropathies and open-heart surgery

      CLINICAL NEUROPHYSIOLOGY
    37. Seeman, P; Mazanec, R; Zidar, J; Hrusakova, S; Ctvrteckova, M; Rautenstrauss, B
      Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy withliability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    38. Muller, HD; Mugler, M; Ramaekers, VT; Schroder, JM
      Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy(HMSN-ADM)

      JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
    39. Rajabally, Y; Vital, A; Ferrer, X; Vital, C; Julien, J; Latour, P; Vandenberghe, A; Lagueny, A
      Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A

      JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
    40. Moudgil, SS; Riggs, JE
      Fulminant peripheral neuropathy with severe quadriparesis associated with vincristine therapy

      ANNALS OF PHARMACOTHERAPY
    41. Mersiyanova, IV; Ismailov, SM; Polyakov, AV; Dadali, EL; Fedotov, VP; Nelis, E; Lofgren, A; Timmerman, V; Van Broeckhoven, C; Evgrafov, OV
      Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32(GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

      HUMAN MUTATION
    42. Senderek, J; Hermanns, B; Lehmann, U; Bergmann, C; Marx, G; Kabus, C; Timmerman, V; Stoltenburg-Didinger, G; Schroder, JM
      Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: Two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met

      BRAIN PATHOLOGY
    43. Colomer, J; Iturriaga, C; Kalaydjieva, L; Angelicheva, D; King, RHM; Thomas, PK
      Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies

      NEUROMUSCULAR DISORDERS
    44. Chandler, D; Angelicheva, D; Heather, L; Gooding, R; Gresham, D; Yanakiev, P; de Jonge, R; Baas, F; Dye, D; Karagyozov, L; Savov, A; Blechschmidt, K; Keats, B; Thomas, PK; King, RHM; Starr, A; Nikolova, A; Colomer, J; Ishpekova, B; Tournev, I; Urtizberea, JA; Merlini, L; Butinar, D; Chabrol, B; Voit, T; Baethmann, M; Nedkova, V; Corches, A; Kalaydjieva, L
      Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

      NEUROMUSCULAR DISORDERS
    45. Mostacciuolo, ML; Rampoldi, L; Righetti, E; Vazza, G; Schiavon, F; Angelini, C
      Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity

      NEUROMUSCULAR DISORDERS
    46. Berciano, J; Garcia, A; Calleja, J; Combarros, O
      Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication

      NEUROMUSCULAR DISORDERS
    47. Hildebrandt, G; Holler, E; Woenkhaus, M; Quarch, G; Reichle, A; Schalke, B; Andreesen, R
      Acute deterioration of Charcot-Marie-Tooth disease IA (CMT IA) following 2mg of vincristine chemotherapy

      ANNALS OF ONCOLOGY
    48. Bolino, A; Levy, ER; Muglia, M; Conforti, FL; LeGuern, E; Salih, MAM; Georgiou, DM; Hausmanowa-Petrusewicz, I; Mandich, P; Gambardella, A; Quattrone, A; Devoto, M; Monaco, AP
      Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22

      GENOMICS
    49. Fukuda, M; Morimoto, T; Suzuki, Y; Kida, K; Ohnishi, A
      Congenital neuropathy with the absence of large myelinated fibers

      PEDIATRIC NEUROLOGY
    50. Geller, TJ; Connolly, AM; Kotagal, S; Prensky, AL
      Progressive infantile axonal polyneuropathy

      JOURNAL OF CHILD NEUROLOGY
    51. Martini, R
      Animal models for inherited peripheral neuropathies: Chances to find treatment strategies?

      JOURNAL OF NEUROSCIENCE RESEARCH
    52. Barisic, N; Mihatov, I
      Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: Follow-up study

      CROATIAN MEDICAL JOURNAL
    53. Teunissen, LL; Eurelings, M; Notermans, NC; Hop, JW; van Gijn, J
      Quality of life in patients with axonal polyneuropathy

      JOURNAL OF NEUROLOGY
    54. Rozental, R; de Carvalho, AC; Spray, DC
      Nervous system diseases involving gap junctions

      BRAIN RESEARCH REVIEWS
    55. Ressot, C; Bruzzone, R
      Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease

      BRAIN RESEARCH REVIEWS
    56. Abrams, CK; Oh, S; Ri, Y; Bargiello, TA
      Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease

      BRAIN RESEARCH REVIEWS
    57. Auer-Grumbach, M; Wagner, K; Strasser-Fuchs, S; Loscher, WN; Fazekas, F; Millner, M; Hartung, HP
      Clinical predominance of proximal upper limb weakness in CMT1A syndrome

      MUSCLE & NERVE
    58. Bergmann, C; Senderek, J; Hermanns, B; Jauch, A; Janssen, D; Schroder, JM; Karch, D
      Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy

      MUSCLE & NERVE
    59. Ericson, U; Borg, J; Borg, K
      Macro-EMG and muscle biopsy of paretic foot dorsiflexors in Charcot-Marie-Tooth disease

      MUSCLE & NERVE
    60. Boonyapisit, K; Katirji, B
      Multifocal motor neuropathy presenting with respiratory failure

      MUSCLE & NERVE
    61. Lewis, RA; Sumner, AJ; Shy, ME
      Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis

      MUSCLE & NERVE
    62. Notermans, NC; Franssen, H; Eurelings, M; Van der Graaf, Y; Wokke, JHJ
      Diagnostic criteria for demyelinating polyneuropathy associated with monoclonal gammopathy

      MUSCLE & NERVE
    63. Butinar, D; Starr, A; Vatovec, J
      Brainstem auditory evoked potentials and cochlear microphonics in the HMSNfamily with auditory neuropathy

      PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
    64. Leonardis, L; Zidar, J; Popovic, M; Timmerman, V; Lofgren, A; Van Broeckhoven, C; Butinar, D
      Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family

      PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
    65. Auer-Grumbach, M; De Jonghe, P; Wagner, K; Verhoeven, K; Hartung, HP; Timmerman, V
      Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locus

      NEUROLOGY
    66. Auer-Grumbach, M; Wagner, K; Timmerman, V; De Jonghe, P; Hartung, HP
      Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci

      NEUROLOGY
    67. Donaghy, M; Sisodiya, SM; Kennett, R; McDonald, B; Haites, N; Bell, C
      Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    68. Misu, K; Yoshihara, T; Shikama, Y; Awaki, E; Yamamoto, M; Hattori, N; Hirayama, M; Takegami, T; Nakashima, K; Sobue, G
      An axonal form of Charcot-Marie-Tooth disease showing distinctive featuresin association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    69. Auer-Grumbach, M; Loscher, WN; Wagner, K; Petek, E; Korner, E; Offenbacher, H; Hartung, HP
      Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V - A clinical, electrophysiological and genetic study

      BRAIN
    70. Krajewski, KM; Lewis, RA; Fuerst, DR; Turansky, C; Hinderer, SR; Garbern, J; Kamholz, J; Shy, ME
      Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A

      BRAIN
    71. Vance, JM
      The many faces of Charcot-Marie-Tooth disease

      ARCHIVES OF NEUROLOGY
    72. Rogers, T; Chandler, D; Angelicheva, D; Thomas, PK; Youl, B; Tournev, I; Gergelcheva, V; Kalaydjieva, L
      A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23

      AMERICAN JOURNAL OF HUMAN GENETICS
    73. Lupski, JR
      Axonal Chaucot-Marie-Tooth disease and the neurofilament light Gene (NF-L)

      AMERICAN JOURNAL OF HUMAN GENETICS
    74. Mersiyanova, IV; Perepelov, AV; Polyakov, AV; Sitnikov, VF; Dadali, EL; Oparin, RB; Petrin, AN; Evgrafov, OV
      A new variant of Charcot-Marie-Tooth disease type 2 is probably the resultof a mutation in the neurofilament-light gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    75. Teunissen, LL; Notermans, NC; Jansen, GH; Banga, JD; Veldman, H; Wokke, JHJ
      Thickness of endoneurial vessel basal lamina area in chronic idiopathic axonal polyneuropathy

      ACTA NEUROPATHOLOGICA
    76. Fabrizi, GM; Taioli, F; Cavallaro, T; Rigatelli, F; Simonati, A; Mariani, G; Perrone, P; Rizzuto, N
      Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero

      ACTA NEUROPATHOLOGICA
    77. Naef, R; Suter, U
      Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies

      NEUROBIOLOGY OF DISEASE
    78. Ben Othmane, K; Johnson, E; Menold, M; Graham, FL; Ben Hamida, M; Hasegawa, O; Rogala, AD; Ohnishi, A; Pericak-Vance, M; Hentati, F; Vance, JM
      Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15

      GENOMICS
    79. Wewetzer, K; Archelos, JJ; Hartung, HP; Seilheimer, B; Christ, B
      The monoclonal antibody 23E9 defines a novel developmentally-regulated Schwann cell surface antigen

      INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE
    80. Pareyson, D
      Guidelines for the diagnosis of Charcot-Marie-Tooth disease and related neuropathies

      ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES
    81. Parman, Y; Plante-Bordeneuve, V; Guiochon-Mantel, A; Eraksoy, M; Said, G
      Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease

      ANNALS OF NEUROLOGY
    82. Scherer, S
      Axonal pathology in demyelinating diseases

      ANNALS OF NEUROLOGY
    83. Neuberg, DHH; Sancho, S; Suter, U
      Altered molecular architecture of peripheral nerves in mice lacking the peripheral myelin protein 22 or connexin32

      JOURNAL OF NEUROSCIENCE RESEARCH
    84. Wulf, P; Bernhardt, RR; Suter, U
      Characterization of peripheral myelin protein 22 in zebrafish (zPMP22) suggests an early role in the development of the peripheral nervous system

      JOURNAL OF NEUROSCIENCE RESEARCH
    85. Donaghy, M; Kennett, R
      Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy

      JOURNAL OF NEUROLOGY
    86. Marques, W; Hanna, MG; Marques, SR; Sweeney, MG; Thomas, PK; Wood, NW
      Phenotypic variation of a new P0 mutation in genetically identical twins

      JOURNAL OF NEUROLOGY
    87. Thomas, PK; Claus, D; King, RHM
      Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy

      JOURNAL OF NEUROLOGY
    88. Dupre, N; Bouchard, JP; Cossette, L; Brunet, D; Vanasse, M; Lemieux, B; Mathon, G; Puymirat, J
      Clinical and electrophysiological study in French-Canadian population withCharcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    89. Heinemeyer, O; Reimers, CD
      Ultrasound of radial, ulnar, median, and sciatic nerves in healthy subjects and patients with hereditary motor and sensory neuropathies

      ULTRASOUND IN MEDICINE AND BIOLOGY
    90. van Erve, RHGP; Driessen, APPM
      Developmental hip dysplasia in hereditary motor and sensory neuropathy type 1

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    91. Castro, C; Gomez-Hernandez, JM; Silander, K; Barrio, LC
      Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations

      JOURNAL OF NEUROSCIENCE
    92. Maki, DD; Yousem, DM; Corcoran, C; Galetta, SL
      MR imaging of Dejerine-Sottas disease

      AMERICAN JOURNAL OF NEURORADIOLOGY
    93. Korinthenberg, R
      Chronic inflammatory demyelinating polyradiculoneuropathy in children and their response to treatment

      NEUROPEDIATRICS
    94. Vital, A; Barat, M; Lagueny, A; Latour, P; Vital, C
      Asymmetrical polyneuropathy with a stepwise progressive course and well-demarcated areas of demyelination

      MUSCLE & NERVE
    95. Tabaraud, F; Lagrange, E; Sindou, P; Vandenberghe, A; Levy, N; Vallat, JM
      Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings

      MUSCLE & NERVE
    96. Sindou, P; Vallat, JM; Chapon, F; Archelos, JJ; Tabaraud, F; Anani, T; Braund, KG; Maisonobe, T; Hauw, JJ; Vandenberghe, A
      Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease

      MUSCLE & NERVE
    97. Tollback, A; Eriksson, S; Wredenberg, A; Jenner, G; Vargas, R; Borg, K; Ansved, T
      Effects of high resistance training in patients with myotonic dystrophy

      SCANDINAVIAN JOURNAL OF REHABILITATION MEDICINE
    98. Stojkovic, T; Latour, P; Vandenberghe, A; Hurtevent, JF; Vermersch, P
      Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)

      NEUROLOGY
    99. Gemignani, F; Marbini, A; Di Giovanni, G; Salih, S; Terzano, MG
      Charcot-Marie-Tooth disease type 2 with restless legs syndrome

      NEUROLOGY
    100. Auer-Grumbach, M; Wagner, K; Fazekas, F; Loscher, WN; Strasser-Fuchs, S; Hartung, HP
      Current classification and genotype-phenotype correlations in hereditary motoric-sensitive neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies

      NERVENARZT


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 01:34:15