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 soggetti phrase all words 'JEWS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 522 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    2. Misbahuddin, A; Warner, TT
      Dystonia: an update on genetics and treatment

      CURRENT OPINION IN NEUROLOGY
    3. Bach, G
      Mucolipidosis type IV

      MOLECULAR GENETICS AND METABOLISM
    4. Patterson, L
      "The living witness of our Redemption": Martyrdom and imitation in Chaucer's 'Prioress's Tale'

      JOURNAL OF MEDIEVAL AND EARLY MODERN STUDIES
    5. Frank, G
      Melville J. Herskovits on the African and Jewish diasporas: Race, culture and modern anthropology

      IDENTITIES-GLOBAL STUDIES IN CULTURE AND POWER
    6. Azoulay, KG
      Jewishness after Mount Sinai: Jews, Blacks and the (multi)racial category

      IDENTITIES-GLOBAL STUDIES IN CULTURE AND POWER
    7. Feldman, JD
      Ghetto association: Jewish heritage, heroin, and racism in Bologna

      IDENTITIES-GLOBAL STUDIES IN CULTURE AND POWER
    8. Goluboff, SL
      The savage in the Jew: Race, class, and nation in post-Soviet Moscow

      IDENTITIES-GLOBAL STUDIES IN CULTURE AND POWER
    9. Touitou, I
      The spectrum of Familial Mediterranean Fever (FMF) mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Bergman, A; Einbeigi, Z; Olofsson, U; Taib, Z; Wallgren, A; Karlsson, P; Wahlstrom, J; Martinsson, T; Nordling, M
      The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Mansour, I; Delague, V; Cazeneuve, C; Dode, C; Chouery, E; Pecheux, C; Medlej-Hashim, M; Salem, N; El Zein, L; Levan-Petit, I; Lefranc, G; Goossens, M; Delpech, M; Amselem, S; Loiselet, J; Grateau, G; Megarbane, A; Naman, R
      Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Creek orthodoxes, Creek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M6941 mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Labrianidis, L
      'Internal frontiers' as a hindrance to development

      EUROPEAN PLANNING STUDIES
    13. Spitzer, J; Hennessy, E; Neville, L
      High group A streptococcal carriage in the orthodox Jewish community of north Hackney

      BRITISH JOURNAL OF GENERAL PRACTICE
    14. Evertsson, S; Lindblom, A; Sun, XF
      APC I1307K and E1317Q variants are rare or do not occur in Swedish colorectal cancer patients

      EUROPEAN JOURNAL OF CANCER
    15. Schiffrin, D
      Language and public memorial: 'America's concentration camps'

      DISCOURSE & SOCIETY
    16. Kaluski, DN; Leventhal, A; Averbuch, Y; Rishpon, S; Cohen-Dar, M; Habib, S; Bellmaker, I; Rubin, L; Rachmiel, S; Amitai, Y; Palti, H
      Five decades of trends in anemia in Israeli infants: implications for foodfortification policy

      EUROPEAN JOURNAL OF CLINICAL NUTRITION
    17. Olopade, OI; Pichert, G
      Cancer genetics in oncology practice

      ANNALS OF ONCOLOGY
    18. Wunderlich, S; Reiners, K; Gasser, T; Naumann, M
      Cervical dystonia in monozygotic twins: Case report and review of the literature

      MOVEMENT DISORDERS
    19. Ben-Zeev, B; Gross, V; Kushnir, T; Shalev, R; Hoffman, C; Shinar, Y; Pras, E; Brand, N
      Vacuolating megalencephalic leukoencephalopathy in 12 Israeli patients

      JOURNAL OF CHILD NEUROLOGY
    20. Baron-Epel, O; Andreev, H; Barhana, M; Green, MS
      Differences in trends of lung carcinoma by histology type in Israeli Jews and Arabs, 1981-1995

      EUROPEAN JOURNAL OF EPIDEMIOLOGY
    21. King, MC; Owens, K
      Genomic views of human history (Reprinted from Science, vol 286, pg 451-453, 1999)

      PATHOLOGIE BIOLOGIE
    22. Kutti, J; Ridell, B
      Epidemiology of the myeloproliferative disorders: essential thrombocythaemia, polycythaemia vera and idiopathic myelofibrosis

      PATHOLOGIE BIOLOGIE
    23. Maurer, T
      A plea for the comparative study of Jewish history in Germany and Eastern Europe

      GESCHICHTE UND GESELLSCHAFT
    24. Major, T; Svetel, M; Romac, S; Kostic, VS
      DYT1 mutation in primary torsion dystonia in a Serbian population

      JOURNAL OF NEUROLOGY
    25. Ghaderi, A; Talei, A; Farjadian, S; Mosalaei, A; Doroudchi, M; Kimura, H
      Germline BRCA1 mutations in Iranian women with breast cancer

      CANCER LETTERS
    26. Al-Arfaj, A
      HLA-DR pattern of rheumatoid arthritis in Saudi Arabia

      ANNALS OF SAUDI MEDICINE
    27. Arnaiz-Villena, A; Elaiwa, N; Silvera, C; Rostom, A; Moscoso, J; Gomez-Casado, E; Allende, L; Varela, P; Martinez-Laso, J
      The origin of Palestinians and their genetic relatedness with other Mediterranean populations

      HUMAN IMMUNOLOGY
    28. Crawford, MH; Reddy, BM; Martinez-Laso, J; Mack, SJ; Erlich, HA
      Genetic variation among the Golla pastoral caste subdivisions of Andhra Pradesh, India, according to the HLA system

      HUMAN IMMUNOLOGY
    29. Gonzalez, S; Brautbar, C; Martinez-Borra, J; Lopez-Vazquez, A; Segal, R; Blanco-Gelaz, MA; Enk, CD; Safriman, C; Lopez-Larrea, C
      Polymorphism in MICA rather than HLA-B/C genes is associated with psoriatic arthritis in the Jewish population

      HUMAN IMMUNOLOGY
    30. Klitz, W; Brautbar, C; Schito, AM; Barcellos, LF; Oksenberg, JR
      Evolution of the CCR5 Delta 32 mutation based on haplotype variation in Jewish and northern European population samples

      HUMAN IMMUNOLOGY
    31. Kwon, OJ; Brautbar, C; Weintrob, N; Sprecher, E; Saphirman, C; Bloch, K; Pinhas-Hamiel, O; Assah, S; Vardi, P; Israel, S
      Immunogenetics of HLA class II in Israeli Ashkenazi Jewish, Israeli non-Ashkenazi Jewish, and in Israeli Arab IDDM patients

      HUMAN IMMUNOLOGY
    32. Dellapergola, S
      Jerusalem's population, 1995-2020: Demography, multiculturalism and urban policies

      EUROPEAN JOURNAL OF POPULATION-REVUE EUROPEENNE DE DEMOGRAPHIE
    33. Goodman, Y
      Dynamics of inclusion and exclusion: Comparing mental illness narratives of Haredi male patients and their rabbis

      CULTURE MEDICINE AND PSYCHIATRY
    34. Weintrob, N; Sprecher, E; Israel, S; Pinhas-Hamiel, O; Kwon, OJ; Bloch, K; Abramov, N; Arbel, A; Josefsberg, Z; Brautbar, C; Vardi, P
      Type I diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in Israel

      DIABETES CARE
    35. Halle, D; Elstein, D; Geudalia, D; Sasson, A; Shinar, E; Schlesinger, M; Zimran, A
      High prevalence of complement C7 deficiency among healthy blood donors of Moroccan Jewish ancestry

      AMERICAN JOURNAL OF MEDICAL GENETICS
    36. Bach, G; Tomczak, J; Risch, N; Ekstein, J
      Tay-sachs screening in the Jewish Ashkenazi population: DNA testing is thepreferred procedure

      AMERICAN JOURNAL OF MEDICAL GENETICS
    37. Schwartz, MD; Rothenberg, K; Joseph, L; Benkendorf, J; Lerman, C
      Consent to the use of stored DNA for genetics research: A survey of attitudes in the Jewish population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    38. Barak, F; Shiri-Svredlov, R; Sade, RBB; Kruglikova, A; Friedman, E; Ben-Dor, D; Goldberg, I
      Adrenal tumors in BRCA1/BRCA2 mutation carriers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    39. Subramanian, G; Adams, MD; Venter, JC; Broder, S
      Implications of the human genome for understanding human biology and medicine

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    40. Zinberg, RE; Kornreich, R; Edelmann, L; Desnick, RJ
      Prenatal genetic screening in the Ashkenazi Jewish population

      CLINICS IN PERINATOLOGY
    41. Suzuki, K
      Recognition and delineation of beta-hexosaminidase alpha-chain variants: Ahistorical and personal perspective

      TAY-SACHS DISEASE
    42. Navon, R
      Late-onset G(M2) gangliosidosis and other hexosaminidase mutations among Jews

      TAY-SACHS DISEASE
    43. Risch, N
      Molecular epidemiology of Tay-Sachs disease

      TAY-SACHS DISEASE
    44. Bar-Tal, D; Labin, D
      The effect of a major event on stereotyping: terrorist attacks in Israel and Israeli adolescents' perceptions of Palestinians, Jordanians and Arabs

      EUROPEAN JOURNAL OF SOCIAL PSYCHOLOGY
    45. Taha, W; Chin, D; Silverberg, AI; Lashiker, L; Khateeb, N; Anhalt, H
      Reduced spinal bone mineral density in adolescents of an ultra-Orthodox Jewish community in Brooklyn

      PEDIATRICS
    46. Carmeli, YS; Birenbaum-Carmeli, D; Madgar, I; Weissenberg, R
      Donor insemination in Israel - Recipients' choice of donor

      JOURNAL OF REPRODUCTIVE MEDICINE
    47. Brik, R; Litmanovitz, D; Berkowitz, D; Shamir, R; Rosenthal, E; Shinawi, M; Gershoni-Baruch, R
      Incidence of familial Mediterranean fever (FMF) mutations among children of Mediterranean extraction with functional abdominal pain

      JOURNAL OF PEDIATRICS
    48. Rosenmann, H; Talmor, G; Halimi, M; Yanai, A; Gabizon, R; Meiner, Z
      Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrPC

      JOURNAL OF NEUROCHEMISTRY
    49. Shaked, GM; Shaked, Y; Kariv-Inbal, Z; Halimi, M; Avraham, I; Gabizon, R
      A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseases

      JOURNAL OF BIOLOGICAL CHEMISTRY
    50. Tomas, C; Picornell, A; Castro, JA; Ramon, MM
      Genetic analyses in five Western Mediterranean populations: Variation at five tetrameric short tandem repeat loci

      HUMAN BIOLOGY
    51. Rochette, B
      Tiberius, the foreign cults and the astrologers (Suetonius, 'Vie de Tibere', 36)

      ETUDES CLASSIQUES
    52. Matsubara, A; Wasson, JC; Donelan, SS; Welling, CM; Glaser, B; Permutt, MA
      Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes

      DIABETOLOGIA
    53. Permutt, MA; Wasson, JC; Suarez, BK; Lin, J; Thomas, J; Meyer, J; Lewitzky, S; Rennich, JS; Parker, A; DuPrat, L; Maruti, S; Chayen, S; Glaser, B
      A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population

      DIABETES
    54. Dossenbach-Glaninger, A; Krugluger, W; Schrattbauer, K; Eder, S; Hopmeier, P
      Severe factor XI deficiency caused by compound heterozygosity for the typeIII mutation and a novel insertion in exon 9 (codons 324/325+G)

      BRITISH JOURNAL OF HAEMATOLOGY
    55. Figer, A; Shtoyerman-Chen, R; Tamir, A; Geva, R; Irmin, L; Flex, D; Theodor, L; Sulkes, A; Sadetzki, S; Bar-Meir, S; Friedman, E
      Phenotypic characteristics of colo-rectal cancer in I1307K APC germline mutation carriers compared with sporadic cases

      BRITISH JOURNAL OF CANCER
    56. Figer, A; Irmin, L; Geva, R; Flex, D; Sulkes, A; Friedman, E
      Genetic analysis of the APC gene regions involved in attenuated APC phenotype in Israeli patients with early onset and familial colorectal cancer

      BRITISH JOURNAL OF CANCER
    57. Chen-Shtoyerman, R; Figer, A; Fidder, HH; Rath, P; Yeremin, L; Bar Meir, S; Friedman, E; Theodor, L
      The frequency of the predominant Jewish mutations in BRCA1 and BRCA2 in unselected Ashkenazi colorectal cancer patients

      BRITISH JOURNAL OF CANCER
    58. Figer, A; Irmin, L; Geva, R; Flex, D; Sulkes, J; Sulkes, A; Friedman, E
      The rate of the 6174delT founder Jewish mutation in BRCA2 in patients withnon-colonic gastrointestinal tract tumours in Israel

      BRITISH JOURNAL OF CANCER
    59. Shea, SH; Wall, TL; Carr, LG; Li, TK
      ADH2 and alcohol-related phenotypes in Ashkenazic Jewish American college students

      BEHAVIOR GENETICS
    60. Warter, JM
      Inherited human prion diseases

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    61. Arnaiz-Villena, A; Karin, M; Bendikuze, N; Gomez-Casado, E; Moscoso, J; Silvera, C; Oguz, FS; Diler, AS; de Pacho, A; Allende, L; Guillen, J; Laso, JM
      HLA alleles and haplotypes in the Turkish population: relatedness to Kurds, Armenians and other Mediterraneans

      TISSUE ANTIGENS
    62. Arnaiz-Villena, A; Dimitroski, K; Pacho, A; Moscoso, J; Gomez-Casado, E; Silvera-Redondo, C; Varela, P; Blagoevska, M; Zdravkovska, V; Martinez-Laso, J
      HLA genes in Macedonians and the sub-Saharan origin of the Greeks

      TISSUE ANTIGENS
    63. Tonin, PN
      Genes implicated in hereditary breast cancer syndromes

      SEMINARS IN SURGICAL ONCOLOGY
    64. Chappuis, PO; Nethercot, V; Foulkes, WD
      Clinico-pathological characteristics of BRCA1-and BRCA2-related breast cancer

      SEMINARS IN SURGICAL ONCOLOGY
    65. Karp, SE
      Clinical management of BRCA1-and BRCA2-associated breast cancer

      SEMINARS IN SURGICAL ONCOLOGY
    66. Ozel, AM; Demirturk, L; Yazgan, Y; Avsar, K; Gunay, A; Gurbuz, AK; Gultepe, M
      Familial Mediterranean fever - A review of the disease and clinical and laboratory findings in 105 patients

      DIGESTIVE AND LIVER DISEASE
    67. Mirabella, M; Christodoulou, K; Di Giovanni, S; Ricci, E; Tonali, P; Servidei, S
      An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1

      NEUROLOGICAL SCIENCES
    68. Zlotogora, J; Leventhal, A
      Screening for genetic disorders among Jews: How should the Tay-Sachs screening program be continued?

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    69. Falik-Zaccai, TC; Shachak, E; Abeliovitch, D; Lerer, I; Shefer, R; Carmi, R; Ries, L; Friedman, M; Shohat, M; Borochowitz, Z
      Achondroplasia in diverse Jewish and Arab populations in Israel: Clinical and molecular characterization

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    70. Mazarib, A; Simon, ES; Korczyn, AD; Falik-Zaccai, Z; Gazit, E; Giladi, N
      Hereditary juvenile-onset craniocervical predominant generalized dystonia with parkinsonism

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    71. Slatkin, M; Rannala, B
      Estimating allele age

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    72. Yair, D; Ben Baruch, G; Chetrit, A; Friedman, T; Yechezkel, GH; Gotlieb, WH; Fishman, A; Beller, U; Bar-Am, A; Friedman, E
      p53 and WAF1 polymorphisms in Jewish-Israeli women with epithelial ovariancancer and its association with BRCA mutations

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    73. Barbagallo, F
      The Rothschilds in Naples (Banking in 19th-century Italian states)

      JOURNAL OF MODERN ITALIAN STUDIES
    74. Bolton-Maggs, PHB
      Factor XI deficiency and its management

      HAEMOPHILIA
    75. Plon, SE; Peterson, LE; Friedman, LC; Richards, CS
      Mammography behavior after receiving a negative BRCA1 mutation test resultin the Ashkenazim: A community-based study

      GENETICS IN MEDICINE
    76. Zlotogora, J; Bach, G; Munnich, A
      Molecular basis of mendelian disorders among Jews

      MOLECULAR GENETICS AND METABOLISM
    77. Ward, CP; Fensom, AH; Green, PM
      Biallelic discrimination assays for the three common Ashkenazi Jewish mutations and a common non-Jewish mutation, in Tay-Sachs disease, using fluorogenic TaqMan probes

      GENETIC TESTING
    78. Tian, HJ; Brody, LC; Landers, JP
      Rapid detection of deletion, insertion, and substitution mutations via heteroduplex analysis using capillary- and microchip-based electrophoresis

      GENOME RESEARCH
    79. Boas, FE
      Linkage to Gaucher mutations in the Ashkenazi population: Effect of drift on decay of linkage disequilibrium and evidence for heterozygote selection

      BLOOD CELLS MOLECULES AND DISEASES
    80. Bouma, BN; Meijers, JCM
      Role of blood coagulation factor XI in downregulation of fibrinolysis

      CURRENT OPINION IN HEMATOLOGY
    81. Grzybowska, E; Zientek, H; Jasinska, A; Rusin, M; Kozlowski, P; Sobczak, K; Sikorska, A; Kwiatkowska, E; Gorniak , L; Kalinowska, E; Utracka-Hutka, B; Wloch, J; Chmielik, E; Krzyzosiak, WJ
      High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer

      HUMAN MUTATION
    82. Shiri-Sverdlov, R; Oefner, P; Green, L; Baruch, RG; Wagner, T; Kruglikova, A; Haitchick, S; Hofstra, RMW; Papa, MZ; Mulder, I; Rizel, S; Sade, RBB; Dagan, E; Abdeen, Z; Goldman, B; Friedman, E
      Mutational analyses of BRCA1 and BRCA2 with Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

      HUMAN MUTATION
    83. Liu, MC; Drury, KC; Kipersztok, S; Zheng, WR; Williams, RS
      Primer system for single cell detection of double mutation for Tay-Sachs disease

      JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
    84. Cui, JS; Hopper, JL
      Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    85. Varese, F; Yaish, M
      The importance of being asked - The rescue of Jews in Nazi Europe

      RATIONALITY AND SOCIETY
    86. Korf, BR
      Integration of genetics into medical practice: ethical, legal, and social perspective

      CURRENT OPINION IN PEDIATRICS
    87. Domingo, C; Touitou, I; Bayou, A; Ozen, S; Notarnicola, C; Dewalle, M; Demaille, J; Buades, R; Sayadat, C; Levy, M; Ben-Chetrit, E
      Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneity

      EUROPEAN JOURNAL OF HUMAN GENETICS
    88. Stoffman, N; Magal, N; Shohat, T; Lotan, R; Koman, S; Oron, A; Danon, Y; Halpern, GJ; Lifshitz, Y; Shohat, M
      Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

      EUROPEAN JOURNAL OF HUMAN GENETICS
    89. Hewett, J; Gonzalez-Agosti, C; Slater, D; Ziefer, P; Li, S; Bergeron, D; Jacoby, DJ; Ozelius, LJ; Ramesh, V; Breakefield, XO
      Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

      HUMAN MOLECULAR GENETICS
    90. Eliakim, R; Reif, S; Lavy, A; Keter, D; Odes, S; Halak, A; Broide, E; Niv, Y; Ron, Y; Paz, J; Fich, A; Villa, Y; Gilat, T
      Passive smoking in patients with inflammatory bowel disease: an Israeli multicentre case-control study

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    91. Tomas, C; Picornell, A; Castro, JA; Ramon, MM; Gusmao, L; Lareu, MV; Carracedo, A
      Genetic variability at nine STR loci in the Chueta (Majorcan Jews) and theBalearic populations investigated by a single multiplex reaction

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    92. Kawaguchi, T; Koga, S; Hongo, H; Komiyama, Y; Li, K; Ishihara, S; Horikawa, K; Hidaka, M; Mitsuya, H; Nakakuma, H
      A novel type of factor XI deficiency showing compound genetic abnormalities: A nonsense mutation and an impaired transcription

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    93. Kono, M; Miyamura, Y; Matsunaga, J; Tomita, Y
      Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9

      JOURNAL OF DERMATOLOGICAL SCIENCE
    94. Tarumi, T; Martincic, D; Whitlock, JA; Addy, JH; Williams, SM; Gailani, D
      Conserved worldwide linkage disequilibrium in the human factor XI gene

      GENOMICS
    95. Munchau, A; Valente, EM; Davis, MB; Stinton, V; Wood, NW; Quinn, NP; Bhatia, KP
      A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia

      MOVEMENT DISORDERS
    96. Hamann, HA; Croyle, RT; Smith, KR; Quan, BNM; McCance, KL; Botkin, JR
      Interest in a support group among individuals tested for a BRCA1 gene mutation

      JOURNAL OF PSYCHOSOCIAL ONCOLOGY
    97. Levy-Lahad, E; Krieger, M; Gottfeld, O; Renbaum, P; Klein, G; Eisenberg, S; Lahad, A; Kaufman, B; Catane, R
      BRCA1 and BRCA2 mutation carriers as potential candidates for chemoprevention trials

      JOURNAL OF CELLULAR BIOCHEMISTRY
    98. Nomura, Y; Ikeuchi, T; Tsuji, S; Segawa, M
      Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia (DYT1) - pathophysiological consideration

      BRAIN & DEVELOPMENT
    99. Simon, ES; Kahana, E; Chapman, J; Treves, TA; Gabizon, R; Rosenmann, H; Zilber, N; Korczyn, AD
      Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutation

      ANNALS OF NEUROLOGY
    100. Sato, E; Kawamata, N; Kato, A; Oshimi, K
      A novel mutation that leads to a congenital factor XI deficiency in a Japanese family

      AMERICAN JOURNAL OF HEMATOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 17/01/21 alle ore 23:24:53