Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' MENDELL JR' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 126 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Tsao, CY; Mendell, JR; Bartholomew, D
      High mitochondrial DNA T8993G mutation (> 90%) without typical features ofLeigh's and NARP syndromes

      JOURNAL OF CHILD NEUROLOGY
    2. Lindenbaum, Y; Kissel, JT; Mendell, JR
      Treatment approaches for Guillian-Barre Syndrome and chronic inflammatory demyelinating polyradiculoneuropathy

      NEUROLOGIC CLINICS
    3. Brown, CA; Lanning, RW; McKinney, KQ; Salvino, AR; Cherniske, E; Crowe, CA; Darras, BT; Gominak, S; Greenberg, CR; Grosmann, C; Heydemann, P; Mendell, JR; Pober, BR; Sasaki, T; Shapiro, F; Simpson, DA; Suchowersky, O; Spence, JE
      Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Kissel, JT; McDermott, MP; Mendell, JR; King, WM; Pandya, S; Griggs, RC; Tawil, R; Cos, L; Langsam, A; Martens, B; Brower, C; Herr, BE; Figlewicz, D; Forrester, J; Downing, K; Holloway, RG; Hubble, J; Kolassa, J
      Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy

      NEUROLOGY
    5. Mendell, JR
      Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy - Reply

      NEUROLOGY
    6. Mendell, JR; Buzin, CH; Feng, J; Yan, J; Serrano, C; Sangani, DS; Wall, C; Prior, TW; Sommer, SS
      Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

      NEUROLOGY
    7. Mendell, JR
      Congenital muscular dystrophy - Searching for a definition after 98 years

      NEUROLOGY
    8. Fenichel, GM; Griggs, RC; Kissel, J; Kramer, TI; Mendell, JR; Moxley, RT; Pestronk, A; Sheng, K; Florence, J; King, WM; Pandya, S; Robison, VD; Wang, H
      A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy

      NEUROLOGY
    9. Musumeci, O; Naini, A; Slonim, AE; Skavin, N; Hadjigeorgiou, GL; Krawiecki, N; Weissman, BM; Tsao, CY; Mendell, JR; Shanske, S; De Vivo, DC; Hirano, M; DiMauro, S
      Familial cerebellar ataxia with muscle coenzyme Q10 deficiency

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

      NEUROLOGY
    11. Mendell, JR; Barohn, RJ; Freimer, ML; Kissel, JT; King, W; Nagaraja, HN; Rice, R; Campbell, WW; Donofrio, PD; Jackson, CE; Lewis, RA; Shy, M; Simpson, DM; Parry, GJ; Rivner, MH; Thornton, CA; Bromberg, MB; Tandan, R; Harati, Y; Giuliani, MJ
      Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy

      NEUROLOGY
    12. Apfel, SC; Asbury, AK; Bril, V; Burns, TM; Campbell, JN; Chalk, CH; Dyck, PJ; Dyck, PJB; Feldman, EL; Fields, HL; Grant, IA; Griffin, JW; Klein, CJ; Lindblom, U; Litchy, WJ; Low, PA; Melanson, M; Mendell, JR; Merren, MD; O'Brien, PC; Rendell, M; Rizza, RA; Service, FJ; Thomas, PK; Walk, D; Wang, AK; Wessel, K; Windebank, AJ; Ziegler, D; Zochodne, DW
      Positive neuropathic sensory symptoms as endpoints in diabetic neuropathy trials

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    13. Tsao, CY; Mendell, JR; Lo, WD; Luquette, M; Rusin, J
      Mitochondrial respiratory-chain defects presenting as nonspecific featuresin children

      JOURNAL OF CHILD NEUROLOGY
    14. Tsao, CY; Mendell, JR; Luquette, M; Dixon, B; Morrow, G
      Mitochondrial DNA depletion in children

      JOURNAL OF CHILD NEUROLOGY
    15. Tsao, CY; Mendell, JR; Lo, WD; Luquette, M; Rennebohm, R
      Myasthenia gravis and associated autoimmune diseases in children

      JOURNAL OF CHILD NEUROLOGY
    16. Tawil, R; McDermott, MP; Brown, R; Shapiro, BC; Ptacek, LJ; McManis, PG; Dalakas, MC; Spector, SA; Mendell, JR; Hahn, AF; Griggs, RC
      Randomized trials of dichlorphenamide in the periodic paralyses

      ANNALS OF NEUROLOGY
    17. Reynolds, JE; Mendell, JR
      Another approach to ventilatory failure in neuromuscular disease

      NEUROLOGY
    18. Collins, MP; Mendell, JR; Periquet, MI; Sahenk, Z; Amato, AA; Gronseth, GS; Barohn, RJ; Jackson, CE; Kissel, JT
      Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy

      NEUROLOGY
    19. Feng, B; Chen, L; Drmanovic, Z; Kakabadze, I; Mendell, JR; Marzluf, GA; Sahenk, Z
      Intracellular processing and toxicity of the truncated androgen receptor: Nuclear congophilia-associated cell death

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    20. Barresi, R; Moore, SA; Stolle, CA; Mendell, JR; Campbell, KP; Campbell, P
      Expression of gamma-sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    21. Sahenk, Z; Chen, L; Mendell, JR
      Effects of PMP22 duplication and deletions on the axonal cytoskeleton

      ANNALS OF NEUROLOGY
    22. Kissel, JT; Mendell, JR
      Muscular dystrophy: Historical overview and classification in the genetic era

      SEMINARS IN NEUROLOGY
    23. Tsao, CY; Mendell, JR
      The childhood muscular dystrophies: Making order out of chaos

      SEMINARS IN NEUROLOGY
    24. Periquet, MI; Novak, V; Collins, MP; Nagaraja, HN; Erdem, S; Nash, SM; Freimer, ML; Sahenk, Z; Kissel, JT; Mendell, JR
      Painful sensory neuropathy - Prospective evaluation using skin biopsy

      NEUROLOGY
    25. Orrell, RW; Tawil, R; Forrester, J; Kissel, JT; Mendell, JR; Figlewicz, DA
      Definitive molecular diagnosis of facioscapulohumeral dystrophy

      NEUROLOGY
    26. Sue, CM; Bruno, C; Andreu, AL; Cargan, A; Mendell, JR; Tsao, CY; Luquette, M; Paolicchi, J; Shanske, S; DiMauro, S; De Vivo, DC
      Infantile encephalopathy associated with the MELAS A3243G mutation

      JOURNAL OF PEDIATRICS
    27. TSAO CY; MENDELL JR; RUSIN J; LUQUETTE M
      CONGENITAL MUSCULAR-DYSTROPHY WITH COMPLETE LAMININ-ALPHA-2-DEFICIENCY, CORTICAL DYSPLASIA, AND CEREBRAL WHITE-MATTER CHANGES IN CHILDREN

      Journal of child neurology
    28. SUE CM; BRUNO C; ANDREU AL; CARGAN A; MENDELL JR; TSAO CY; SHANSKE S; DIMAURO S; DEVIVO DC
      INFANTILE ENCEPHALOPATHY ASSOCIATED WITH THE MELAS A3243G MUTATION

      Annals of neurology
    29. Mendell, JR
      Charcot-Marie-Tooth neuropathies and related disorders

      SEMINARS IN NEUROLOGY
    30. BARTOLO C; MENDELL JR; PRIOR TW
      IDENTIFICATION OF A MISSENSE MUTATION IN A FRIEDREICHS ATAXIA PATIENT- IMPLICATIONS FOR DIAGNOSIS AND CARRIER STUDIES

      American journal of medical genetics
    31. SCIACCO M; GASPARORIPPA P; VU TH; TANJI K; SHANSKE S; MENDELL JR; SCHON EA; DIMAURO S; BONILLA E
      STUDY OF MITOCHONDRIAL-DNA DEPLETION IN MUSCLE BY SINGLE-FIBER POLYMERASE-CHAIN-REACTION

      Muscle & nerve
    32. BRADLEY WG; DAUBE J; MENDELL JR; POSNER J; RICHMAN D; TROOST BT; SWIFT TR
      QUALITY IMPROVEMENT IN NEUROLOGY RESIDENCY PROGRAMS - REPLY

      Neurology
    33. KISSEL JT; MCDERMOTT MP; NATARAJAN R; MENDELL JR; PANDYA S; KING WM; GRIGGS RC; TAWIL R
      PILOT TRIAL OF ALBUTEROL IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

      Neurology
    34. KAKABADZE I; MENDELL JR; SAHENK Z
      ALTERATIONS IN NODES OF RANVIER AND SCHMIDT-LANTERMAN INCISURES IN CHARCOT-MARIE-TOOTH NEUROPATHIES

      Neurology
    35. SAHENK Z; ERDEM S; MENDELL JR
      FATE OF SCHWANN-CELLS IN CMT1A - EVIDENCE FOR APOPTOSIS

      Neurology
    36. MENDELL JR; PERIQUET I; KISSEL JT; NASH SM; FREIMER ML; SAHENK Z; NOVAK V
      DISTAL PAINFUL AXONAL IDIOPATHIC NEUROPATHY - CRITERIA FOR DIAGNOSIS AND DISTINCTION FROM OTHER SENSORY NEUROPATHIES

      Neurology
    37. ERDEM S; FREIMER ML; ODORISIO T; MENDELL JR
      PROCAINAMIDE-INDUCED CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY

      Neurology
    38. ERDEM S; MENDELL JR; SAHENK Z
      FATE OF SCHWANN-CELLS IN CMT1A AND HNPP - EVIDENCE FOR APOPTOSIS

      Journal of neuropathology and experimental neurology
    39. Parsons, DW; McAndrew, PE; Iannaccone, ST; Mendell, JR; Burghes, AHM; Prior, TW
      Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number

      AMERICAN JOURNAL OF HUMAN GENETICS
    40. COOVERT DD; LE TT; MCANDREW PE; STRASSWIMMER J; CRAWFORD TO; MENDELL JR; COULSON SE; ANDROPHY EJ; PRIOR TW; BURGHES AHM
      THE SURVIVAL MOTOR-NEURON PROTEIN IN SPINAL MUSCULAR-ATROPHY

      Human molecular genetics
    41. FOUAD G; DALAKAS M; SERVIDEI S; MENDELL JR; VANDENBERGH P; ANGELINI C; ALDERSON K; GRIGGS RC; TAWIL R; GREGG R; HOGAN K; POWERS PA; WEINBERG N; MALONEE W; PTACEK LJ
      GENOTYPE-PHENOTYPE CORRELATIONS OF DHP RECEPTOR ALPHA(1)-SUBUNIT GENE-MUTATIONS CAUSING HYPOKALEMIC PERIODIC PARALYSIS

      Neuromuscular disorders
    42. ORRELL RW; FORRESTER JD; TAWIL R; KISSEL JT; MENDELL JR; FIGLEWICZ DA; GRIGGS RC
      APPLICATION OF DEFINITIVE MOLECULAR DIAGNOSTIC-CRITERIA IN FACIOSCAPULOHUMERAL DYSTROPHY - CLINICAL IMPLICATIONS OF POSITION EFFECT VARIEGATION

      Annals of neurology
    43. COLLINS MP; MENDELL JR; PERIQUET MI; SAHENK Z; AMATO AA; KISSEL JT
      IMMUNOSTAINING IN VASCULITIC NEUROPATHY - SENSITIVITY AND SPECIFICITYOF FINDINGS

      Annals of neurology
    44. ERDEM S; PERIQUET MI; NASH SM; DOWNING KA; COLLINS MP; FREIMER ML; KISSEL JT; MENDELL JR
      ASSESSMENT OF EPIDERMAL NERVE-FIBERS TO DETERMINE THE PATHOBIOLOGY OFAGING

      Annals of neurology
    45. GRIGGS RC; TAWIL R; BROWN RH; SHAPIRO BE; PTACEK L; MCMANIS PG; DALAKAS MC; MENDELL JR; HALM AF; MCDERMOTT MP
      DICHLORPHENAMIDE IS EFFECTIVE IN THE TREATMENT OF HYPOKALEMIC PERIODIC PARALYSIS

      Annals of neurology
    46. DIDONATO CJ; INGRAHAM SE; MENDELL JR; PRIOR TW; LENARD S; MOXLEY RT; FLORENCE J; BURGHES AHM
      DELETION AND CONVERSION IN SPINAL MUSCULAR-ATROPHY PATIENTS - IS THERE A RELATIONSHIP TO SEVERITY

      Annals of neurology
    47. BRADLEY WG; DAUBE J; MENDELL JR; POSNER J; RICHMAN D; TROOST BT; SWIFT TR
      QUALITY IMPROVEMENT IN NEUROLOGY RESIDENCY PROGRAMS - REPORT OF THE QUALITY IMPROVEMENT COMMITTEE OF THE ASSOCIATION OF UNIVERSITY PROFESSORS OF NEUROLOGY

      Neurology
    48. COLLINS MP; KISSEL JT; PERIQUET IM; SAHENK Z; BAROHN RJ; AMATO AA; JACKSON CE; MENDELL JR
      SUPERFICIAL PERONEAL NERVE PERONEUS BREVIS MUSCLE BIOPSIES IN MULTIFOCAL NEUROPATHIES - PREDICTIVE VALUES OF PATHOLOGICAL FEATURES ASSOCIATED WITH NECROTIZING VASCULITIS

      Neurology
    49. KISSEL JT; MENDELL JR; GRIGGS RC; MCDERMOTT M; TAWIL R
      OPEN-LABEL CLINICAL-TRIAL OF ALBUTEROL IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

      Neurology
    50. MENDELL JT; FENG B; SAHENK Z; MARZLUF GA; AMATO AA; MENDELL JR
      NOVEL LAMININ ALPHA-2 MUTATIONS IN CONGENITAL MUSCULAR-DYSTROPHY

      Neurology
    51. SAHENK Z; CHEN L; MONANI U; MENDELL JR
      STUDIES ON THE EFFECT OF PMP22 DUPLICATION AND DELETION ON AXONAL CYTOSKELETON USING NERVE XENOGRAFT MODEL

      Neurology
    52. PRIOR TW; BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; KISSEL JT; LUQUETTE MH; TSAO CY; MENDELL JR
      DYSTROPHIN EXPRESSION IN A DUCHENNE MUSCULAR-DYSTROPHY PATIENT WITH AFRAME-SHIFT DELETION

      Neurology
    53. TAWIL R; GRIGGS RC; MCDERMOTT MP; COS L; PERSONIUS KE; LANGSAM A; PANDYA S; MARONIAN A; SASS A; MCCOY K; BROWER CA; PLUMB S; MARTENS W; HERR BE; FORRESTER J; FIGLEWICZ D; MENDELL JR; KISSEL J; RAINEY F; DOWNING K; KING WM
      A PROSPECTIVE, QUANTITATIVE STUDY OF THE NATURAL-HISTORY OF FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) - IMPLICATIONS FOR THERAPEUTIC TRIALS

      Neurology
    54. TAWIL R; MCDERMOTT MP; PANDYA S; KING W; KISSEL J; MENDELL JR; GRIGGS RC; COS L; LANGSAM A; MARTENS B; BROWER C; HERR BE; FIGLEWICZ D; FORRESTER J; DOWNING K
      A PILOT TRIAL OF PREDNISONE IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

      Neurology
    55. PRIOR TW; MCANDREW PE; PARSONS DW; PAPP AC; SNYDER PJ; SEDRA MS; SCHAFER RW; HEINZ JW; MENDELL JR; BURGHES AHM
      RESULTS OF DOSAGE SCREENING THE SMN GENE FOR CARRIER AND DIAGNOSTIC TESTING

      American journal of human genetics
    56. COOVERT DD; LE T; MCANDREW PE; STRASSWIMMER J; CRAWFORD TO; MENDELL JR; ANDROPHY E; PRIOR TW; BURGHES AHM
      THE SURVIVAL MOTOR-NEURON PROTEIN (SMN) IN SPINAL MUSCULAR-ATROPHY (SMA)

      American journal of human genetics
    57. MCANDREW PE; PARSONS DW; MENDELL JR; BURGHES AHM; PRIOR TW
      PREVALENCE OF APPARENT GENE CONVERSION EVENTS IN SPINAL MUSCULAR-ATROPHY

      American journal of human genetics
    58. MCANDREW PE; PARSONS DW; SIMARD LR; ROCHETTE C; RAY PN; MENDELL JR; PRIOR TW; BURGHES AHM
      IDENTIFICATION OF PROXIMAL SPINAL MUSCULAR-ATROPHY CARRIERS AND PATIENTS BY ANALYSIS OF SMNT AND SMNC GENE COPY NUMBER

      American journal of human genetics
    59. MENDELL JR; GARCHA TS; KISSEL JT
      THE IMMUNOPATHOGENIC ROLE OF COMPLEMENT IN HUMAN MUSCLE DISEASE

      Current opinion in neurology
    60. PRIOR TW; BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR
      NONSENSE MUTATIONS IN A BECKER MUSCULAR-DYSTROPHY AND AN INTERMEDIATEPATIENT

      Human mutation
    61. PARSONS DW; MCANDREW PE; MONANI UR; MENDELL JR; BURGHES AHM; PRIOR TW
      AN 11 BASE-PAIR DUPLICATION IN EXON-6 OF THE SMN GENE PRODUCES A TYPE-I SPINAL MUSCULAR-ATROPHY (SMA) PHENOTYPE - FURTHER EVIDENCE FOR SMN AS THE PRIMARY SMA-DETERMINING GENE

      Human molecular genetics
    62. KISSEL JT; MENDELL JR
      NEUROPATHIES ASSOCIATED WITH MONOCLONAL GAMMOPATHIES

      Neuromuscular disorders
    63. SAHENK Z; GOEL A; BARNETT D; MENDELL JR
      MOLECULAR-GENETIC DEFECT IN MUSCLE AMP-DEAMINASE DEFICIENCY - RELATIONSHIP PHENOTYPE

      Annals of neurology
    64. COLLINS MP; KISSEL JT; SAHENK Z; BAROHN RJ; AMTO AA; JACKSON CE; MENDELL JR
      DIAGNOSTIC-VALUE OF COMBINED SUPERFICIAL PERONEAL NERVE PERONEUS BREVIS MUSCLE BIOPSY IN SUSPECTED VASCULITIS

      Annals of neurology
    65. SANTORELLI FM; SCIACCO M; TANJI K; SHANSKE S; VU TH; GOLZI V; GRIGGS RC; MENDELL JR; HAYS AP; BERTORINI TE; PESTRONK A; BONILLA E; DIMAURO S
      MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN SPORADIC INCLUSION-BODY MYOSITIS - A STUDY OF 56 PATIENTS

      Annals of neurology
    66. CORNBLATH DR; BRAINE HG; DYCK PJ; MENDELL JR; RODRIGUEZ M; ROPPER AH; WOLINSKY JS; FERGUSON JH; ALTROCCHI PH; BRIN M; GOLDMAN RS; GOLDSTEIN M; GOODIN DS; GORELICK PB; HANLEY DF; LANGE J; MARINI AM; NUWER MR; ROACH ES; VANDENNOORT S
      ASSESSMENT OF PLASMAPHERESIS

      Neurology
    67. KISSEL JT; MENDELL JR; GRIGGS RC; MCDERMOTT MP; TAWIL R
      THE EFFECTS OF A BETA(2) AGONIST ON MUSCLE MASS IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

      Neurology
    68. TSAO CY; BARTOLO C; LUQUETTE MH; MENDELL JR; PRIOR TW
      A NOVEL MECHANISM FOR THE EXPRESSION OF DYSTROPHIN IN A DUCHENNE MUSCULAR-DYSTROPHY PATIENT

      Neurology
    69. MENDELL JR; FREIMER M; KISSEL JT; GUILIANI M; NEWMAN D; KING W; DOWNING K; RICE R; NAGARAJA H; TALLEY S; BOWMAN R; WOOLLETT L; WISNE S
      RANDOMIZED, DOUBLE-BLIND CROSSOVER TRIAL OF ANDROGEN HORMONE DEFICIENCY AND REPLACEMENT IN X-LINKED BULBAR SPINAL MUSCULAR-ATROPHY

      Neurology
    70. BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; HALL CD; MENDELL JR; PRIOR TW
      A NOVEL SPLICE-SITE MUTATION IN A BECKER MUSCULAR-DYSTROPHY PATIENT

      Journal of Medical Genetics
    71. THOMPSON TG; DIDONATO CJ; SIMARD LR; INGRAHAM SE; BURGHES AHM; CRAWFORD TO; ROCHETTE C; MENDELL JR; WASMUTH JJ
      A NOVEL CDNA DETECTS HOMOZYGOUS MICRODELETIONS IN GREATER-THAN 50-PERCENT OF TYPE-I SPINAL MUSCULAR-ATROPHY PATIENTS

      Nature genetics
    72. TSAO CY; LO WD; MENDELL JR; BATLEY RJ
      CRITICAL ILLNESS POLYNEUROPATHY IN A 2-YEAR-OLD GIRL WITH HEMORRHAGIC-SHOCK ENCEPHALOPATHY SYNDROME

      Journal of child neurology
    73. MENDELL JR; SAHENK Z; PRIOR TW
      THE CHILDHOOD MUSCULAR-DYSTROPHIES - DISEASES SHARING A COMMON PATHOGENESIS OF MEMBRANE INSTABILITY

      Journal of child neurology
    74. GRIGGS RC; ASKANAS V; DIMAURO S; ENGEL A; KARPATI G; MENDELL JR; ROWLAND LP
      INCLUSION-BODY MYOSITIS AND MYOPATHIES

      Annals of neurology
    75. MENDELL JR
      MITOCHONDRIAL MYOPATHY IN THE ELDERLY - EXAGGERATED AGING IN THE PATHOGENESIS OF DISEASE

      Annals of neurology
    76. NADKARNI N; FREIMER M; MENDELL JR
      CASE OF THE MONTH - AMYLOIDOSIS CAUSING A PROGRESSIVE MYOPATHY

      Muscle & nerve
    77. MENDELL JR; KISSEL JT; AMATO AA; KING W; SIGNORE L; PRIOR TW; SAHENK Z; BESSON S; MCANDREW PE; RICE R; NAGARAJA H; STEPHENS R; LANTRY L; MORRIS GE; BURGHES AHM
      MYOBLAST TRANSFER IN THE TREATMENT OF DUCHENNES MUSCULAR-DYSTROPHY

      The New England journal of medicine
    78. BAROHN RJ; AMATO AA; SAHENK Z; KISSEL JT; MENDELL JR
      INCLUSION-BODY MYOSITIS - EXPLANATION FOR POOR RESPONSE TO IMMUNOSUPPRESSIVE THERAPY

      Neurology
    79. SCIACCO M; GASPARORIPPA P; SHANSKE S; MENDELL JR; SCHON EA; DIMAURO S; BONILLA E
      LATE-ONSET MUSCLE MITOCHONDRIAL-DNA (MTDNA) DEPLETION - DIAGNOSIS BY SINGLE-FIBER PCR

      Neurology
    80. GUIDA M; MARGER RS; PAPP AC; SNYDER PJ; SEDRA MS; KISSEL JT; MENDELL JR; PRIOR TW
      A MOLECULAR PROTOCOL FOR DIAGNOSING MYOTONIC-DYSTROPHY

      Clinical chemistry
    81. TAN E; LYNN DJ; AMATO AA; KISSEL JT; RAMMOHAN KW; SAHENK Z; WARMOLTS JR; JACKSON CE; BAROHN RJ; MENDELL JR
      IMMUNOSUPPRESSIVE TREATMENT OF MOTOR-NEURON SYNDROMES - REPLY

      Archives of neurology
    82. PRIOR TW; BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR
      SPECTRUM OF SMALL MUTATIONS IN THE DYSTROPHIN CODING REGION

      American journal of human genetics
    83. BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR; PRIOR TW
      NOVEL MUTATIONS AND THE MOLECULAR MECHANISM OF MILDLY AFFECTED MUSCULAR-DYSTROPHY PATIENTS

      American journal of human genetics
    84. FIGLEWICZ DA; FORRESTER J; MCDERMOTT MP; MENDELL JR; KISSEL J; GRIGGS RC; TAWIL R
      ANALYSIS OF GENOTYPE-PHENOTYPE CORRELATION IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)

      American journal of human genetics
    85. PRIOR TW; BARTOLO C; PEARL DK; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR
      SPECTRUM OF SMALL MUTATIONS IN THE DYSTROPHIN CODING REGION

      American journal of human genetics
    86. WINNARD AV; MENDELL JR; PRIOR TW; FLORENCE J; BURGHES AHM
      FRAMESHIFT DELETIONS OF EXONS-3-7 AND REVERTANT FIBERS IN DUCHENNE MUSCULAR-DYSTROPHY - MECHANISMS OF DYSTROPHIN PRODUCTION

      American journal of human genetics
    87. NADKARNI N; PRIOR TW; MENDELL JR
      THE IMPACT OF MOLECULAR-GENETICS ON THE CARE OF PATIENTS WITH MUSCLE DISEASE

      Current opinion in neurology
    88. PRIOR TW; BARTOLO C; PAPP AC; SNYDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR
      IDENTIFICATION OF A MISSENSE MUTATION, SINGLE-BASE DELETION AND A POLYMORPHISM IN THE DYSTROPHIN EXON-16

      Human molecular genetics
    89. BAROHN RJ; BRUMBACK RA; MENDELL JR
      HYALINE BODY MYOPATHY

      Neuromuscular disorders
    90. BURGHES AHM; INGRAHAM SE; KOTEJARAI Z; ROSENFELD S; HERTA N; NADKARNI N; DIDONATO CJ; CARPTEN J; HURKO O; FLORENCE J; MOXLEY RT; COBBEN JM; MENDELL JR
      LINKAGE MAPPING OF THE SPINAL MUSCULAR-ATROPHY GENE

      Human genetics
    91. LYNN DJ; WODA RP; MENDELL JR
      RESPIRATORY DYSFUNCTION IN MUSCULAR-DYSTROPHY AND OTHER MYOPATHIES

      Clinics in chest medicine
    92. PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; WESTERN LM; BARTOLO C; MOXLEY RT; MENDELL JR
      HETERODUPLEX ANALYSIS OF THE DYSTROPHIN GENE - APPLICATION TO POINT MUTATION AND CARRIER DETECTION

      American journal of medical genetics
    93. PTACEK LJ; TAWIL R; GRIGGS RC; MEOLA G; MCMANIS P; BAROHN RJ; MENDELL JR; HARRIS C; SPITZER R; SANTIAGO F; LEPPERT MF
      SODIUM-CHANNEL MUTATIONS IN ACETAZOLAMIDE-RESPONSIVE MYOTONIA-CONGENITA, PARAMYOTONIA-CONGENITA, AND HYPERKALEMIC PERIODIC PARALYSIS

      Neurology
    94. SANTORELLI FM; SCIACCO M; SHANSKE S; GRIGGS RC; MENDELL JR; BONILLA E; DIMAURO S
      MITOCHONDRIAL-DNA DELETIONS IN PATIENTS WITH INCLUSION-BODY MYOSITIS

      Neurology
    95. SEHARASYON J; SAHENK Z; MENDELL JR; BURGHES AHM
      DELIVERY OF ADENOVIRUS-BASED GENE CONSTRUCTS IN SPINAL MOTOR-NEURONS VIA RETROGRADE AXONAL-TRANSPORT

      Neurology
    96. TAWIL R; MCDERMOTT MP; MENDELL JR; KISSEL J; GRIGGS RC
      THE NATURAL-HISTORY OF FSHD

      Neurology
    97. COOVERT DD; MCANDREW PE; SAHENK Z; MENDELL JR; BURGHES AHM
      ADENOVIRAL MEDIATED TRANSFER OF BETA-GALACTOSIDASE AND DYSTROPHIN CONSTRUCTS TO MUSCLE

      Neurology
    98. MENDELL JR; KISSEL JT; STEVENS R; LANTRY L; AMATO T; KING W; SIGNORE L; RICE R; NAGARAJA HN; PAN G; PRIOR T; BURGHES A
      PROSPECTIVE, CONTROLLED TRIAL OF 6 MONTHLY MYOBLAST TRANSFERS IN DUCHENNE DYSTROPHY

      Neurology
    99. SAHENK Z; SAHARSEYON J; MENDELL JR
      CILIARY NEUROTROPHIC FACTOR (CNTF) POTENTIATES PERIPHERAL-NERVE REGENERATION

      Neurology
    100. PRIOR TW; BARTOLO C; PAPP AC; SYNDER PJ; SEDRA MS; BURGHES AHM; MENDELL JR
      IDENTIFICATION OF NEW MUTATIONS IN BECKER INTERMEDIATE MUSCULAR-DYSTROPHY PATIENTS/

      Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/08/20 alle ore 13:37:51