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    1. Shimoyama, T; Fukuda, S; Tanaka, M; Nakaji, S; Fukuda, Y; Munakata, A
      Evaluation of the association between serum anti-Lewis X antibody and inflammatory infiltration into the gastric mucose infected with Helicobacter pylori

      DIGESTIVE AND LIVER DISEASE
    2. Stephens, HAF
      MICA and MICB genes: can the enigma of their polymorphism be resolved?

      TRENDS IN IMMUNOLOGY
    3. Nagata, H; Kumahara, K; Tomemori, T; Arimoto, Y; Isoyama, K; Yoshida, K; Konno, A
      Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics

      JOURNAL OF HUMAN GENETICS
    4. Lieb, K; Staeheli, P
      Borna disease virus - does it infect humans and cause psychiatric disorders?

      JOURNAL OF CLINICAL VIROLOGY
    5. Ueno, Y; Ishii, M; Igarashi, T; Mano, Y; Yahagi, K; Kisara, N; Kobayashi, Y; Niitsuma, H; Kobayashi, K; Shimosegawa, T
      Primary biliary cirrhosis with antibody against carbonic anhydrase II associates with distinct immunological backgrounds

      HEPATOLOGY RESEARCH
    6. Mochizuki, H; Kamakura, K; Masaki, T; Hirata, A; Tokuda, T; Yazaki, M; Motoyoshi, K; Ikeda, S
      Nodular cutaneous amyloidosis and carpal tunnel syndrome due to the amyloidogenic transthyretin His 114 variant

      AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
    7. Tang, S; Lai, KN
      Gene polymorphism in IgA nephropathy

      NEPHROLOGY
    8. Moulds, JM
      Ethnic diversity of class III genes in autoimmune disease

      FRONTIERS IN BIOSCIENCE
    9. Richt, JA; Rott, R
      Borna disease virus: a mystery as an emerging zoonotic pathogen

      VETERINARY JOURNAL
    10. Maximo, V; Soares, P; Seruca, R; Rocha, AS; Castro, P; Sobrinho-Simoes, M
      Microsatellite instability, mitochondrial DNA large deletions, and mitochondrial DNA mutations in gastric carcinoma

      GENES CHROMOSOMES & CANCER
    11. Bolognesi, E; D'Alfonso, S; Rolando, V; Fasano, ME; Pratico, L; Momigliano-Richiardi, R
      MICA and MICB microsatellite alleles in HLA extended haplotypes

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    12. Caraco, Y; Muszkat, M; Wood, AJJ
      Phenytoin metabolic ratio: a putative marker of CYP2C9 activity in vivo

      PHARMACOGENETICS
    13. van der Weide, J; Steijns, LSW; van Weelden, MJM; de Haan, K
      The effect of genetic polymorphism of cytochrome P450CYP2C9 on phenytoin dose requirement

      PHARMACOGENETICS
    14. Klemm, T; Neumann, S; Trulzsch, B; Pistrosch, F; Hanefeld, M; Paschke, R
      Search for mitochondrial DNA, mutation ate position 3243 in German patients with a positive family history of maternal diabetes mellitus

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    15. Yeromenko, Y; Lavie, L; Levy, Y
      Homocysteine and cardiovascular risk in patients with diabetes mellitus

      NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
    16. Tsuboi, K; Iida, S; Kato, M; Hayami, Y; Hanamura, I; Miura, K; Harada, S; Komatsu, H; Banno, S; Wakita, A; Nitta, M; Ueda, R
      Improvement of splenomegaly and pancytopenia by enzyme replacement therapyagainst type 1 Gaucher disease: A report of sibling cases

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    17. Tanaka, N; Saito, H; Ito, T; Momose, K; Ishida, F; Hora, K; Kiyosawa, K; Ida, H
      Initiation of enzyme replacement therapy for an adult patient with asymptomatic type 1 Gaucher's disease

      INTERNAL MEDICINE
    18. Singal, DP; Li, J; Zhang, G
      Microsatellite polymorphism of the MICA gene and susceptibility to rheumatoid arthritis

      CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
    19. Frontali, M
      Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?

      BRAIN RESEARCH BULLETIN
    20. Yang, X; Aoki, Y; Li, X; Sakamoto, O; Hiratsuka, M; Kure, S; Taheri, S; Christensen, E; Inui, K; Kubota, M; Ohira, M; Ohki, M; Kudoh, J; Kawasaki, K; Shibuya, K; Shintani, A; Asakawa, S; Minoshima, S; Shimizu, N; Narisawa, K; Matsubara, Y; Suzuki, Y
      Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency

      HUMAN GENETICS
    21. Sakamoto, O; Ohura, T; Katsushima, Y; Fujiwara, I; Ogawa, E; Miyabayashi, S; Iinuma, K
      A novel intronic mutation of the TAZ (G4.5) gene in a patient with Barth syndrome: creation of a 5 ' splice donor site with variant GC consensus and elongation of the upstream exon

      HUMAN GENETICS
    22. Tsuge, T; Shimokawa, T; Horikoshi, S; Tomino, Y; Ra, C
      Polymorphism in promoter region of Fc alpha receptor gene in patients withIgA nephropathy

      HUMAN GENETICS
    23. Bolstad, AI; Wassmuth, R; Haga, HJ; Jonsson, R
      HLA markers and clinical characteristics in Caucasians with primary Sjogren's syndrome

      JOURNAL OF RHEUMATOLOGY
    24. Kang, SH; Park, MH; Song, EY; Kang, SJ; Lee, EB; Song, YW; Takeuchi, F
      Association of HLA class II genes with systemic sclerosis in Koreans

      JOURNAL OF RHEUMATOLOGY
    25. Yokota, K; Shimizu, H
      Psoriasis vulgaris associated with Vogt-Koyanagi-Harada Syndrome

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    26. Makita, Y; Tomino, Y
      Genetic background: Patients

      TYPE-2 DIABETIC NEPHROPATHY IN JAPAN: FROM BENCH TO BEDSIDE
    27. Nishi, S; Ueno, M; Gejyo, F
      Renal biopsy findings and clinical course

      TYPE-2 DIABETIC NEPHROPATHY IN JAPAN: FROM BENCH TO BEDSIDE
    28. Kim, HS; Yoon, SK; Cho, BJ; Kim, EK; Joo, CK
      BIGH3 gene mutations and rapid detection in Korean patients with corneal dystrophy

      CORNEA
    29. Wiencke, K; Spurkland, A; Schrumpf, E; Boberg, KM
      Primary sclerosing cholangitis is associated to an extended B8-DR3 haplotype including particular MICA and MICB alleles

      HEPATOLOGY
    30. Rubio, CA; Jonasson, JG; Filipe, I; Cabanne, AM; Hojman, R; Kogan, Z; Nesi, G; Amorosi, A; Zampi, G; Klimstra, D
      Gastric carcinomas of intestinal type concur with distant changes in the gastric mucose. A multicenter study in the Atlantic Basin

      ANTICANCER RESEARCH
    31. Choukri, F; Chakib, A; Himmich, H; Hue, S; Caillat-Zucman, S
      HLA-B*51 and B*15 alleles confer predisposition to Behcet's disease in Moroccan patients

      HUMAN IMMUNOLOGY
    32. Gonzalez, R; Storr, M; Bloching, H; Seige, M; Ott, R; Allescher, HD
      Autoantibody profile in progressive systemic sclerosis as markers for esophageal involvement

      JOURNAL OF CLINICAL GASTROENTEROLOGY
    33. Caca, K; Ferenci, P; Kuhn, HJ; Polli, C; Willgerodt, H; Kunath, B; Hermann, W; Mossner, J; Berr, F
      High prevalence of the H1069Q mutation in East German patients with Wilsondisease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis

      JOURNAL OF HEPATOLOGY
    34. Kato, T; Kameoka, S; Kimura, T; Soga, N; Abe, Y; Nishikawa, T; Kobayashi, M
      Angiogenesis as a predictor of long-term survival for 377 Japanese patients with breast cancer

      BREAST CANCER RESEARCH AND TREATMENT
    35. Kato, T; Kameoka, S; Kimura, T; Nishikawa, T; Kasajima, T
      Angiogenesis and blood vessel invasion as prognostic indicators for node-negative breast cancer

      BREAST CANCER RESEARCH AND TREATMENT
    36. Kubo, S; Tamori, A; Ohba, K; Shuto, T; Yamamoto, T; Tanaka, H; Nishiguchi, S; Wakasa, K; Hirohashi, K; Kinoshita, H
      Previous or occult hepatitis B virus infection in hepatitis C virus-associated hepatocellular carcinoma without hepatic fibrosis

      DIGESTIVE DISEASES AND SCIENCES
    37. Taniwaki, H; Ishimura, E; Matsumoto, N; Emoto, M; Inaba, M; Nishizawa, Y
      Relations between ACE gene and ecNOS gene polymorphisms and resistive index in type 2 diabetic patients with nephropathy

      DIABETES CARE
    38. Meigs, JB; Jacques, PF; Selhub, J; Singer, DE; Nathan, DM; Rifai, N; D'Agostino, RB; Wilson, PWF
      Fasting plasma homocysteine levels in the insulin resistance syndrome - The Framingham Offspring Study

      DIABETES CARE
    39. Ng, MCY; Lee, SC; Ko, GTC; Li, JKY; So, WY; Hashim, Y; Barnett, AH; Mackay, IR; Critchley, JAJH; Cockram, CS; Chan, JCN
      Familial early-onset type 2 diabetes in Chinese patients - Obesity and genetics have more significant roles than autoimmunity

      DIABETES CARE
    40. Seki, H; Kubota, T; Ikegawa, S; Haga, N; Fujioka, F; Ohzeki, S; Wakui, K; Yoshikawa, H; Takaoka, K; Fukushima, Y
      Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Azizah, MR; Ainol, SS; Kuak, SH; Kong, NCT; Normaznah, Y; Rahim, MN
      The association of the HLA class II antigens with clinical and autoantibody expression in Malaysian Chinese patients with systemic lupus erythematosus

      ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY
    42. Gex-Fabry, M; Balant-Gorgia, AE; Balant, LP
      Therapeutic drug monitoring databases for postmarketing surveillance of drug-drug interactions

      DRUG SAFETY
    43. Kim, JS; Nafziger, AN; Gaedigk, A; Dickmann, LJ; Rettie, AE; Bertino, JS
      Effects of oral vitamin K on S- and R-Warfarin pharmacokinetics and pharmacodynamics: Enhanced safety of warfarin as a CYP2C9 probe

      JOURNAL OF CLINICAL PHARMACOLOGY
    44. Batlle, D; Ghanekar, H; Jain, S; Mitra, A
      Hereditary distal renal tubular acidosis: New understandings

      ANNUAL REVIEW OF MEDICINE
    45. Yoon, BW; Bae, HJ; Kang, DW; Lee, SH; Hong, KS; Kim, KB; Park, BJ; Roh, JK
      Intracranial cerebral artery disease as at risk factor for central nervoussystem complications of coronary artery bypass graft surgery

      STROKE
    46. Hasegawa, Y; Kaneoka, H; Tanaka, T; Ogahara, S; Matsumae, T; Noda, R; Yoshitake, K; Murata, T; Naito, S
      Suppression of experimental membranous glomerulonephritis in rats by an anti-MHC class II antibody

      NEPHRON
    47. Galla, JH
      Molecular genetics in IgA nephropathy

      NEPHRON
    48. Solans, R; Labrador, M; Bosch, JA
      Epidemiology and pathogenesis of Sjogren's syndrome

      MEDICINA CLINICA
    49. Al-Khalidi, JA; Czaja, AJ
      Current concepts in the diagnosis, pathogenesis, and treatment of autoimmune hepatitis

      MAYO CLINIC PROCEEDINGS
    50. Kono, T; Nishimura, F; Sugimoto, H; Sikata, K; Makino, H; Murayama, Y
      Human fibroblasts ubiquitously express glutamic acid decarboxylase 65 (GAD65): Possible effects of connective tissue inflammation on GAD antibody titer

      JOURNAL OF PERIODONTOLOGY
    51. Lee, MH; Hazard, S; Carpten, JD; Yi, S; Cohen, Y; Gerhardt, GT; Salen, G; Patel, SB
      Fine-mapping, mutation analyses, and structural mapping of cerebrotendinous xanthomatosis in US pedigrees

      JOURNAL OF LIPID RESEARCH
    52. Watanabe, H; Enomoto, N; Nagayama, K; Izumi, N; Marumo, F; Sato, C; Watanabe, M
      Number and position of mutations in the interferon (IFN) sensitivity-determining region of the gene for nonstructural protein 5A correlate with IFN efficacy in hepatitis C virus genotype 1b infection

      JOURNAL OF INFECTIOUS DISEASES
    53. Zhou, XD; Tan, FK; Xiong, MM; Milewicz, DM; Feghali, CA; Fritzler, MJ; Reveille, JD; Arnett, FC
      Systemic sclerosis (scleroderma): Specific autoantigen genes are selectively overexpressed in scleroderma fibroblasts

      JOURNAL OF IMMUNOLOGY
    54. Jang, GF; Van Hooser, JP; Kuksa, V; McBee, JK; He, YG; Janssen, JJM; Driessen, CAGG; Palczewski, K
      Characterization of a dehydrogenase activity responsible for oxidation of 11-cis-retinol in the retinal pigment epithelium of mice with a disrupted RDH5 gene - A model for the human hereditary disease fundus albipunctatus

      JOURNAL OF BIOLOGICAL CHEMISTRY
    55. Donaldson, P; Agarwal, K; Craggs, A; Craig, W; James, O; Jones, D
      HLA and interleukin 1 gene polymorphisms in primary biliary cirrhosis: associations with disease progression and disease susceptibility

      GUT
    56. Norris, S; Kondeatis, E; Collins, R; Satsangi, J; Clare, M; Chapman, R; Stephens, H; Harrison, P; Vaughan, R; Donaldson, P
      Mapping MHC-encoded susceptibility and resistance in primary sclerosing cholangitis: The role of MICA polymorphism

      GASTROENTEROLOGY
    57. Thijssen, HHW; Drittij, MJ; Vervoort, LMT; de Vries-Hanje, JC
      Altered pharmacokinetics of R- and S-acenocoumarol in a subject heterozygous for CYP2C9*3

      CLINICAL PHARMACOLOGY & THERAPEUTICS
    58. Liu, TT; Chiang, SH; Wu, SJ; Hsiao, KJ
      Tetrahydrobiopterin-deficient hyperphenylalaninemia in the Chinese

      CLINICA CHIMICA ACTA
    59. Itoyama, A; Chaganti, RSK; Yamada, Y; Tsukasaki, K; Atogami, S; Nakamura, H; Tomonaga, M; Ohshima, K; Kikuchi, M; Sadamori, N
      Cytogenetic analysis and clinical significance in adult T-cell leukemia/lymphoma: a study of 50 cases from the human T-cell leukemia virus type-1 endemic area, Nagasaki

      BLOOD
    60. Nishiguchi, N; Matsushita, S; Suzuki, K; Murayama, M; Shirakawa, O; Higuchi, S
      Association between 5HT2A receptor gene promoter region polymorphism and eating disorders in Japanese patients

      BIOLOGICAL PSYCHIATRY
    61. Wu, ZY; Wang, N; Lin, MT; Fang, L; Murong, SX; Yu, L
      Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease

      ARCHIVES OF NEUROLOGY
    62. Sinke, RJ; Ippel, EF; Diepstraten, CM; Beemer, FA; Wokke, JHJ; van Hilten, BJ; Knoers, NVAM; van Amstel, HKP; Kremer, HPH
      Clinical and molecular correlations in spinocerebellar ataxia type 6 - A study of 24 Dutch families

      ARCHIVES OF NEUROLOGY
    63. Tabarin, A
      Congenital adrenal hypoplasia and DAX-1 gene mutations

      ANNALES D ENDOCRINOLOGIE
    64. Duclos-Vallee, JC; Johanet, C; Sebagh, M; Samuel, D; Yamamoto, AM
      Autoimmune hepatitis: mecanisms, clinical, pathological and therapeutic features

      ANNALES DE MEDECINE INTERNE
    65. Okano, Y; Asada, M; Fujimoto, A; Ohtake, A; Murayama, K; Hsiao, KJ; Choeh, K; Yang, YL; Cao, QX; Reichardt, JKV; Niihira, S; Imamura, T; Yamano, T
      A genetic factor for age-related cataract: Identification and characterization of a novel galactokinase variant, "Osaka," in Asians

      AMERICAN JOURNAL OF HUMAN GENETICS
    66. Czaja, AJ
      Understanding the pathogenesis of autoimmune hepatitis

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    67. Shiono, Y; Wakusawa, S; Hayashi, H; Takikawa, T; Yano, M; Okada, T; Mabuchi, H; Kono, S; Miyajima, H
      Iron accumulation in the liver of male patients with Wilson's disease

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    68. Tanaka, A; Borchers, AT; Ishibashi, H; Ansari, AA; Keen, CL; Gershwin, ME
      Genetic and familial considerations of primary biliary cirrhosis

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    69. Ortlepp, JR; Breithardt, O; Ohme, F; Hanrath, P; Hoffmann, R
      Lack of association polymorphisms and cardiac among five genetic of the renin-angiotensin system hypertrophy in patients with aortic stenosis

      AMERICAN HEART JOURNAL
    70. Macchia, PE
      Recent advances in understanding the molecular basis of primary congenitalhypothyroidism

      MOLECULAR MEDICINE TODAY
    71. Trepo, C
      Genotype and viral load as prognostic indicators in the treatment of hepatitis C

      JOURNAL OF VIRAL HEPATITIS
    72. Wilson, C; Tiwana, H; Ebringer, A
      Molecular mimicry between HLA-DR alleles associated with rheumatoid arthritis and Proteus mirabilis as the aetiological basis for autoimmunity

      MICROBES AND INFECTION
    73. Marre, M; Hadjadj, S; Bouhanick, B
      Hereditary factors in the development of diabetic renal disease

      DIABETES & METABOLISM
    74. Jarvis, B; Spencer, CM
      Management of hypertension in patients with diabetes mellitus - Defining the role of lisinopril

      DISEASE MANAGEMENT & HEALTH OUTCOMES
    75. Folkerth, RD; Alroy, J; Bhan, I; Kaye, EM
      Infantile G(M1) gangliosidosis complete morphology and histochemistry of two autopsy cases, with particular reference to delayed central nervous system myelination

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    76. Freedman, BI; Satko, SG
      Genes and renal disease

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    77. Morrone, A; Bardelli, T; Donati, MA; Giorgi, M; Di Rocco, M; Gatti, R; Parini, R; Ricci, R; Taddeucci, G; D'Azzo, A; Zammarchi, E
      beta-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement

      HUMAN MUTATION
    78. Stone, DL; Tayebi, N; Orvisky, E; Stubblefield, B; Madike, V; Sidransky, E
      Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

      HUMAN MUTATION
    79. Fujiwara, H; Tatsumi, K; Tanaka, S; Kimura, M; Nose, O; Amino, N
      A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect

      THYROID
    80. Spitzweg, C; Heufelder, AE; Morris, JC
      Thyroid iodine transport

      THYROID
    81. Alvarez, I; de Castro, JAL
      HLA-B27 and immunogenetics of spondyloarthropathies

      CURRENT OPINION IN RHEUMATOLOGY
    82. Molassiotis, A
      A pilot study of the use of progressive muscle relaxation training in the management of post-chemotherapy nausea and vomiting

      EUROPEAN JOURNAL OF CANCER CARE
    83. Franke, W; Neumann, NJ; Ruzicka, T; Schulte, KW
      Plantar malignant melanoma - a challenge for early recognition

      MELANOMA RESEARCH
    84. Thijssen, HHW; Verkooijen, IWC; Frank, HLL
      The possession of the CYP2C9*3 allele is associated with low dose requirement of acenocoumarol

      PHARMACOGENETICS
    85. Takanashi, K; Tainaka, H; Kobayashi, K; Yasumori, T; Hosakawa, M; Chiba, K
      CYP2C9 Ile(359) and Leu(359) variants: enzyme kinetic study with seven substrates

      PHARMACOGENETICS
    86. Okada, T; Morise, T; Takeda, Y; Mabuchi, H
      A new variant deletion of a copper-transporting P-type ATPase gene found in patients with Wilson's disease presenting with fulminant hepatic failure

      JOURNAL OF GASTROENTEROLOGY
    87. Tomiyama, Y
      Glanzmann thrombasthenia: Integrin alpha(IIb)beta(3) deficiency

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    88. Luisetti, M; Beretta, A; Casali, L
      Genetic aspects in sarcoidosis

      EUROPEAN RESPIRATORY JOURNAL
    89. Itoh, Y; Igarashi, T; Tatsuma, N; Imai, T; Yoshida, J; Tsuchiya, M; Murakami, M; Fukunaga, Y
      Immunogenetic background of patients with autoimmune fatigue syndrome

      AUTOIMMUNITY
    90. Spitzweg, C; Morris, JC
      The immune response to the iodide transporter

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    91. Hazama, H; Omagari, K; Masuda, J; Kinoshita, H; Ohba, K; Sakimura, A; Matsuo, I; Isomoto, H; Murase, K; Murata, I; Kohno, S
      Serial changes in enzyme inhibitory antibody to pyruvate dehydrogenase complex during the course of primary biliary cirrhosis

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    92. Nishizawa, Y; Tanaka, E; Orii, K; Rokuhara, A; Ichijo, T; Yoshizawa, K; Kiyosawa, K
      Clinical impact of genotype 1 TT virus infection in patients with chronic hepatitis C and response of TT virus to alpha-interferon

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    93. Wu, ZY; Wang, N; Murong, SX; Lin, MT
      Identification and analysis of mutations of the Wilson disease gene in Chinese population

      CHINESE MEDICAL JOURNAL
    94. Yamashita, I; Sasaki, H; Yabe, I; Fukazawa, T; Nogoshi, S; Komeichi, K; Takada, A; Shiraishi, K; Takiyama, Y; Nishizawa, M; Kaneko, J; Tanaka, H; Tsuji, S; Tashiro, K
      A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter

      ANNALS OF NEUROLOGY
    95. Uemura, K; Nakura, J; Kohara, K; Miki, T
      Association of ACE I/D polymorphism with cardiovascular risk factors

      HUMAN GENETICS
    96. Loke, KY; Larry, KSP; Lee, YS; Peter, M; Drop, SLS
      Prepubertal diagnosis of X-linked congenital adrenal hypoplasia presentingafter infancy

      EUROPEAN JOURNAL OF PEDIATRICS
    97. Mattey, DL; Gonzalez-Gay, MA; Hajeer, AH; Dababneh, A; Thomson, W; Garcia-Porrua, C; Ollier, WER
      Association between HLA-DRB1*15 and secondary Sjogren's syndrome in patients with rheumatoid arthritis

      JOURNAL OF RHEUMATOLOGY
    98. Konishi, M; Yamada, M; Nakamura, Y; Mashima, Y
      Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene

      CURRENT EYE RESEARCH
    99. Chayama, K; Suzuki, F; Tsubota, A; Kobayashi, M; Arase, Y; Saitoh, S; Suzuki, Y; Murashima, N; Ikeda, K; Takahashi, N; Kinoshita, M; Kumada, H
      Association of amino acid sequence in the PKR-eIF2 phosphorylation homology domain and response to interferon therapy

      HEPATOLOGY
    100. Duvic, C; Sarret, D; De Revel, T; Herody, M; Didelot, F; Labaye, J; Nedelec, G
      IgD myeloma with acute renal failure.

      REVUE DE MEDECINE INTERNE


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Documento generato il 10/12/19 alle ore 14:53:58