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    1. Erlandson, A; Hallberg, B; Hagberg, B; Wahlstrom, J; Martinsson, T
      MECP2 mutation screening in Swedish classical Rett syndrome females

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    2. 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
    3. Einbeigi, Z; Bergman, A; Kindblom, LG; Martinsson, T; Meis-Kindblom, JM; Nordling, M; Suurkula, M; Wahlstrom, J; Wallgren, A; Karlsson, P
      A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer

      EUROPEAN JOURNAL OF CANCER
    4. Astuti, D; Agathanggelou, A; Honorio, S; Dallol, A; Martinsson, T; Kogner, P; Cummins, C; Neumann, HPH; Voutilainen, R; Dahia, P; Eng, C; Maher, ER; Latif, F
      RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

      ONCOGENE
    5. Gabre, P; Martinsson, T; Gahnberg, L
      Longitudinal study of dental caries, tooth mortality and interproximal bone loss in adults with intellectual disability

      EUROPEAN JOURNAL OF ORAL SCIENCES
    6. Erlandson, A; Bjursell, C; Stibler, H; Kristiansson, B; Wahlstrom, J; Martinsson, T
      Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations

      HUMAN GENETICS
    7. Schilling, FH; Ambros, PF; Bihl, H; Martinsson, T; Ambros, IM; Borgstrom, P; Jacobsson, H; Falkmer, UG; Treuner, J; Kogner, P
      Absence of somatostatin receptor expression in vivo is correlated to di- or tetraploid 1p36-deleted neuroblastomas

      MEDICAL AND PEDIATRIC ONCOLOGY
    8. Ejeskar, K; Sjoberg, RM; Abel, F; Kogner, P; Ambros, PF; Martinsson, T
      Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours

      MEDICAL AND PEDIATRIC ONCOLOGY
    9. Strandvik, B; Gronowitz, E; Enlund, F; Martinsson, T; Wahlstrom, J
      Essential fatty acid deficiency in relation to genotype in patients with cystic fibrosis

      JOURNAL OF PEDIATRICS
    10. Gabre, P; Wikstrom, M; Martinsson, T; Gahnberg, L
      Move of adults with mental retardation from institutions to community-based living: Changes in the oral microbiological flora

      JOURNAL OF DENTAL RESEARCH
    11. Bjork, J; Akerbrant, H; Iselius, L; Bergman, A; Engwall, Y; Wahlstrom, J; Martinsson, T; Nordling, M; Hultcrantz, R
      Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations

      GASTROENTEROLOGY
    12. Gronert, K; Martinsson-Niskanen, T; Ravasi, S; Chiang, N; Serhan, CN
      Selectivity of recombinant human leukotriene D-4, leukotriene B-4, and lipoxin A(4) receptors with aspirin-triggered 15-epi-LXA(4) and regulation of vascular and inflammatory responses

      AMERICAN JOURNAL OF PATHOLOGY
    13. Erlandson, A; Stibler, H; Kristiansson, B; Wahlstrom, J; Martinsson, T
      Denaturing high-performance liquid chromatography is a suitable method forPMM2 mutation screening in carbohydrate-deficient glycoprotein syndrome type IA patients

      GENETIC TESTING
    14. Matthijs, G; Schollen, E; Bjursell, C; Erlandson, A; Freeze, H; Imtiaz, F; Kjaergaard, S; Martinsson, T; Schwartz, M; Seta, N; Vuillaumier-Barrot, S; Westphal, V; Winchester, B
      Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

      HUMAN MUTATION
    15. Bjursell, C; Erlandson, A; Nordling, M; Nilsson, S; Wahlstrom, J; Stibler, H; Kristiansson, B; Martinsson, T
      PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

      HUMAN MUTATION
    16. Jogi, A; Abel, F; Sjoberg, RM; Toftgard, R; Zaphiropoulos, PG; Pahlman, S; Martinsson, T; Axelson, H
      Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    17. Enerback, C; Nilsson, S; Enlund, F; Inerot, A; Samuelsson, L; Wahlstrom, J; Swanbeck, G; Martinsson, T
      Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patients

      ARCHIVES OF DERMATOLOGICAL RESEARCH
    18. Ejeskar, K; Abel, F; Sjoberg, RM; Backstrom, J; Kogner, P; Martinsson, T
      Fine mapping of the human preprocortistatin gene (CORT) to neuroblastoma consensus deletion region 1p36.3 -> p36.2, but absence of mutations in primary tumors

      CYTOGENETICS AND CELL GENETICS
    19. Schilling, FH; Bihl, H; Jacobsson, H; Ambros, PF; Martinsson, T; Borgstrom, P; Schwarz, K; Ambros, IM; Treuner, J; Kogner, P
      Combined In-111-pentetreotide scintigraphy and I-123-mIBG scintigraphy in neuroblastoma provides prognostic information

      MEDICAL AND PEDIATRIC ONCOLOGY
    20. Martinsson, T; Oldfors, A; Darin, N; Berg, K; Tajsharghi, H; Kyllerman, M; Wahlstrom, J
      Autosomal dominant myopathy: Missense mutation (Glu-706 -> Lys) in the myosin heavy chain IIa gene

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    21. Enerback, C; Enlund, F; Inerot, A; Samuelsson, L; Wahlstrom, J; Swanbeck, G; Martinsson, T
      S gene (Corneodesmosin) diversity and its relationship to psoriasis; High content of cSNP in the HLA-linked S gene

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    22. Jansson, M; Darin, N; Kyllerman, M; Martinsson, T; Wahlstrom, J; Oldfors, A
      Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

      ACTA NEUROPATHOLOGICA
    23. Naluai, AT; Nilsson, S; Samuelsson, L; Gudjonsdottir, AH; Ascher, H; Ek, J; Hallberg, B; Kristiansson, B; Martinsson, T; Nerman, O; Sollid, LM; Wahlstrom, J
      The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders

      TISSUE ANTIGENS
    24. Ejeskar, K; Sjoberg, RM; Kogner, P; Martinsson, T
      Variable expression and absence of mutations in p73 in primary neuroblastoma tumors argues against a role in neuroblastoma development

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    25. Enlund, F; Samuelsson, L; Enerback, C; Inerot, A; Wahlstrom, J; Yhr, M; Torinsson, A; Riley, J; Swanbeck, G; Martinsson, T
      Psoriasis susceptibility locus in chromosome region 3q21 identified in patients from southwest Sweden

      EUROPEAN JOURNAL OF HUMAN GENETICS
    26. Enerback, C; Holmqvist, D; Inerot, A; Enlund, F; Samuelsson, L; Torinsson, A; Wahlstrom, J; Swanbeck, G; Martinsson, T
      Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11q

      EUROPEAN JOURNAL OF HUMAN GENETICS
    27. Samuelsson, L; Enlund, F; Torinsson, A; Yhr, M; Inerot, A; Enerback, C; Wahlstrom, J; Swanbeck, G; Martinsson, T
      A genome-wide search for genes predisposing to familial psoriasis by usinga stratification approach

      HUMAN GENETICS
    28. Einbeigi, Z; Kindblom, J; Kindblom, LG; Martinsson, T; Suurkula, M; Wahlstrom, J; Wallgren, A; Karlsson, P
      A founder mutation of the BRCA1-gene in Western Sweden

      DISEASE MARKERS
    29. Martinsson, T; Ljung, T; Rubio, C; Hellstrom, PM
      Beneficial effects of ropivacaine in rat experimental colitis

      JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
    30. Martinsson, T
      Ropivacaine inhibits serum-induced proliferation of colon adenocarcinoma cells in vitro

      JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
    31. Wahlstrom, J; Uller, A; Johannesson, T; Holmqvist, D; Darnfors, C; Vujic, M; Tonnby, B; Hagberg, B; Martinsson, T
      Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p

      JOURNAL OF MEDICAL GENETICS
    32. Frostad, B; Martinsson, T; Tani, E; Falkmer, U; Darnfors, C; Skoog, L; Kogner, P
      The use of fine-needle aspiration cytology in the molecular characterization of neuroblastoma in children

      CANCER CYTOPATHOLOGY
    33. Abel, F; Ejeskar, K; Kogner, P; Martinsson, T
      Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2 (SSTR2) gene at 17q24

      BRITISH JOURNAL OF CANCER
    34. Martinsson, T; Darin, N; Kyllerman, M; Oldfors, A; Hallberg, B; Wahlstrom, J
      Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosomeregion 17p13.1

      AMERICAN JOURNAL OF HUMAN GENETICS
    35. Gabre, P; Martinsson, T; Gahnberg, L
      Simplified sampling methods for estimating levels of lactobacilli in saliva in dental clinical practice

      ACTA ODONTOLOGICA SCANDINAVICA
    36. Gabre, P; Martinsson, T; Gahnberg, L
      Incidence of, and reasons for, tooth mortality among mentally retarded adults during a 10-year period

      ACTA ODONTOLOGICA SCANDINAVICA
    37. Enlund, F; Samuelsson, L; Enerback, C; Inerot, A; Wahlstrom, J; Yhr, M; Torinsson, A; Martinsson, T; Swanbeck, G
      Analysis of three suggested psoriasis susceptibility loci in a large Swedish set of families: Confirmation of linkage to chromosome 6p (HLA region), and to 17q, but not to 4q

      HUMAN HEREDITY
    38. Bjursell, C; Wahlstrom, J; Berg, K; Stibler, H; Kristiansson, B; Matthijs, G; Martinsson, T
      Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families

      EUROPEAN JOURNAL OF HUMAN GENETICS
    39. KJAERGAARD S; KRISTIANSSON B; STIBLER H; FREEZE HH; SCHWARTZ M; MARTINSSON T; SKOVBY F
      FAILURE OF SHORT-TERM MANNOSE THERAPY OF PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE 1A

      Acta paediatrica
    40. DARIN N; KYLLERMAN M; WAHLSTROM J; MARTINSSON T; OLDFORS A
      AUTOSOMAL-DOMINANT MYOPATHY WITH CONGENITAL JOINT CONTRACTURES, OPHTHALMOPLEGIA, AND RIMMED VACUOLES

      Annals of neurology
    41. HOLM G; MARTINSSON T
      THE SWEDISH NATIONAL DENTAL INSURANCES PERIODONTAL DIAGNOSIS - USED ON AN INDIVIDUAL-LEVEL

      Swedish dental journal
    42. ROOSAAR A; AXELL T; MARTINSSON T
      A 20-YEARS FOLLOW-UP-STUDY OF ORAL MUCOSAL CHANGES - PRELIMINARY-REPORT

      Journal of dental research
    43. NORDLING M; KARLSSON P; WAHLSTROM J; ENGWALL Y; WALLGREN A; MARTINSSON T
      A LARGE DELETION DISRUPTS THE EXON-3 TRANSCRIPTION ACTIVATION DOMAIN OF THE BRCA2 GENE IN A BREAST OVARIAN CANCER FAMILY/

      Cancer research
    44. Ejeskar, K; Aburatani, H; Abrahamsson, J; Kogner, P; Martinsson, T
      Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumour-suppressor locus distal to the FHIT gene

      BRITISH JOURNAL OF CANCER
    45. GEVORGIAN S; MARTINSSON T; DELENIV A; KOLLBERG E; VENDIK I
      SIMPLE AND ACCURATE DISPERSION EXPRESSION FOR THE EFFECTIVE DIELECTRIC-CONSTANT OF COPLANAR WAVE-GUIDES

      IEE proceedings. Microwaves, antennas and propagation
    46. MARTINSSON T; HAEGERSTRAND A; DALSGAARD CJ
      EFFECTS OF ROPIVACAINE ON EICOSANOID RELEASE FROM HUMAN GRANULOCYTES AND ENDOTHELIAL-CELLS IN-VITRO

      Inflammation research
    47. WIKLUND L; NORDLING M; WAHLSTROM J; ENGWALL Y; MARTINSSON T
      NOVEL GERMLINE MUTATIONS IN SWEDISH VON-HIPPEL-LINDAU DISEASE PATIENTS - CORRELATION TO CLINICAL MANIFESTATIONS

      International journal of oncology
    48. WAHLSTROM J; ULLER A; TONNBY B; DARNFORS C; MARTINSSON T; VUJIC M; HAGBERG B
      CONGENITAL RETT-SYNDROME PHENOTYPE - DELETION SHORT ARM CHROMOSOME-3

      European child & adolescent psychiatry
    49. HALLSTENSSON K; THULIN S; ABURATANI H; HIPPO Y; MARTINSSON T
      REPRESENTATIONAL DIFFERENCE ANALYSIS AND LOSS OF HETEROZYGOSITY STUDIES DETECT 3P DELETIONS IN NEUROBLASTOMA

      European journal of cancer
    50. MARTINSSON T; SJOBERG RM; HALLSTENSSON K; NORDLING M; HEDBORG F; KOGNER P
      DELIMITATION OF A CRITICAL TUMOR-SUPPRESSOR REGION AT DISTAL 1P IN NEUROBLASTOMA TUMORS

      European journal of cancer
    51. BJURSELL C; STIBLER H; WAHLSTROM J; KRISTIANSSON B; SKOVBY F; STROMME P; BLENNOW G; MARTINSSON T
      FINE MAPPING OF THE GENE FOR CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I (CDG1) - LINKAGE DISEQUILIBRIUM AND FOUNDER EFFECT IN SCANDINAVIAN FAMILIES

      Genomics
    52. HENRY S; JOVALL PA; GHARDASHKHANI S; ELMGREN A; MARTINSSON T; LARSON G; SAMUELSSON B
      STRUCTURAL AND IMMUNOCHEMICAL IDENTIFICATION OF LE(A), LE(B), H-TYPE-1, AND RELATED GLYCOLIPIDS IN SMALL-INTESTINAL MUCOSA OF A GROUP-O LE(A-B-) NONSECRETOR

      Glycoconjugate journal
    53. NORDLING M; ENGWALL Y; WAHLSTROM J; WIKLUND L; ERIKSSON MA; GUSTAVSSON B; FASTH S; LARSSON PA; MARTINSSON T
      NOVEL MUTATIONS IN THE APC GENE AND CLINICAL-FEATURES IN SWEDISH PATIENTS WITH POLYPOSIS-COLI

      Anticancer research
    54. MARTINSSON T; SJOBERG RM; HEDBORG F; KOGNER P
      HOMOZYGOUS DELETION OF THE NEUROFIBROMATOSIS-1 GENE IN THE TUMOR OF APATIENT WITH NEUROBLASTOMA

      Cancer genetics and cytogenetics
    55. MARTINSSON T; ODA T; FERNVIK E; ROEMPKE K; DALSGAARD CJ; SVENSJO E
      ROPIVACAINE INHIBITS LEUKOCYTE ROLLING, ADHESION AND CD11B CD18 EXPRESSION/

      The Journal of pharmacology and experimental therapeutics
    56. ENERBACK C; MARTINSSON T; INEROT A; WAHLSTROM J; ENLUND F; YHR M; SAMUELSSON L; SWANBECK G
      SIGNIFICANTLY EARLIER AGE AT ONSET FOR THE HLA-CW6-POSITIVE THAN FOR THE CW6-NEGATIVE PSORIATIC SIBLING

      Journal of investigative dermatology
    57. BORNSTEIN R; ZIMMERMAN M; MARTINSSON T
      DENTAL ATTENDANCE AND DENTAL-HEALTH AMONG COMPANY EMPLOYEES

      Journal of dental research
    58. SWANBECK G; INEROT A; MARTINSSON T; ENERBACK C; ENLUND F; SAMUELSSON L; YHR M; WAHLSTROM J
      GENETIC-COUNSELING IN PSORIASIS - EMPIRICAL-DATA ON PSORIASIS AMONG FIRST-DEGREE RELATIVES OF 3095 PSORIATIC PROBANDS

      British journal of dermatology
    59. BJURSELL C; WAHLSTROM J; STIBLER H; KRISTIANSSON B; MATTHIJS G; MARTINSSON T
      PRENATAL DIAGNOSTIC-TOOLS FOR ANALYSIS OF SCANDINAVIAN CDG TYPE-I PATIENTS

      American journal of human genetics
    60. ENLUND F; SAMUELSSON L; ENERBACK C; INEROT A; WAHLSTROM J; YHR M; TORINSSON A; MARTINSSON T; SWANBECK G
      ANALYSIS OF 3 SUGGESTED PSORIASIS SUSCEPTIBILITY LOCI IN A LARGE SWEDISH MATERIAL - LINKAGE TO CHROMOSOME 6P (HLA-REGION) AND TO 17Q, BUT NOT TO 4Q

      American journal of human genetics
    61. ENERBACK C; MARTINSSON T; INEROT A; WAHLSTROM J; ENLUND F; YHR M; SAMUELSSON L; SWANBECK G
      DIFFERENT AGE AT ONSET FOR PSORIATIC SIBLINGS DISCORDANT FOR THE PRESENCE OF CW6 AT THE HLA-C LOCUS

      American journal of human genetics
    62. ENERBACK C; MARTINSSON T; INEROT A; WAHLSTROM J; ENLUND F; YHR M; SWANBECK G
      EVIDENCE THAT HLA-CW6 DETERMINES EARLY-ONSET OF PSORIASIS, OBTAINED USING SEQUENCE-SPECIFIC PRIMERS (PCR-SSP)

      Acta dermato-venereologica
    63. GEVORGIAN S; DELENIV A; MARTINSSON T; GALCHENKO S; LINNER P; VENDIK I
      CAD MODEL OF A GAP IN A COPLANAR WAVE-GUIDE

      International journal of microwave and millimeter-wave computer-aided engineering
    64. SJOBERG RM; HALLSTENSSON K; NORDLING M; KOGNER P; GARDELLIN P; LUBYOVA B; ONYANGO P; WEITH A; MARTINSSON T
      ANALYSIS OF LOCATION AND INTEGRITY OF THE HUMAN PITSLRE (P58(CDC2L1))GENES IN NEUROBLASTOMA CELL GENOMES - EVIDENCE AGAINST INVOLVEMENT INTUMORIGENESIS

      International journal of oncology
    65. MARTINSSON T; JOHANNESSON T; VUJIC M; SJOSTEDT A; STEFFENBURG S; GILLBERG C; WAHLSTROM J
      MATERNAL ORIGIN OF INV DUP(15) CHROMOSOMES IN INFANTILE-AUTISM

      European child & adolescent psychiatry
    66. NAYLOR SL; CARRITT B; BOILEAU C; BEROUD C; ALEXANDER C; ALLDERDICE P; ALIMOV A; ASHWORTH T; BONIFAS J; BUGERT P; BUYS CHCM; CHIPPERFIELD MA; DENG G; DRABKIN H; GEMMILL RM; GROMPE M; JOENSUU T; JONASDOTTIR A; GIZATULLIN R; KROIS L; LEACH RJ; LOTT ST; KILLARY A; MARTINSSON T; MESSIAEN L; OCONNELL P; OPALKA B; PLAETKE R; SANKILA EM; SMITH DI; STRACHEN T; VANDENBERG A; ZABAROVSKY E
      REPORT OF THE 6TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-3 MAPPING 1995 - HELD ON 23-24 OCTOBER 1995 - MINNEAPOLIS, MINNESOTA

      Cytogenetics and cell genetics
    67. MARTINSSON T; SJLBERG R; HALLSTENSSON K; NORDLING M; KOGNER P; GARDELLIN P; LUBYOVA B; ONYANGO P; WEITH A
      PITSLRE (P58CDC2L1) GENES IN NEUROBLASTOMA CELL GENOMES - EVIDENCE AGAINST INVOLVEMENT IN TUMORIGENESIS

      Cytogenetics and cell genetics
    68. MARTINSSON T; SJOBERG RM; HALLSTENSSON K; HEDBORG F; KOGNER P
      ANALYSIS OF 1P-DELETIONS IN NEUROBLASTOMA TUMORS - DELIMITATION OF THE CRITICAL REGION WITH GENETICALLY MAPPED SHORT TANDEM REPEAT POLYMORPHISMS

      Cytogenetics and cell genetics
    69. BERGKVIST M; MARTINSSON T; AMAN P; SANDBERGWOLLHEIM M
      NO GENETIC-LINKAGE BETWEEN MULTIPLE-SCLEROSIS AND THE INTERFERON-ALPHA BETA LOCUS/

      Journal of neuroimmunology
    70. GEVORGIAN SS; MARTINSSON T; LINNER PLJ; KOLLBERG EL
      CAD MODELS FOR MULTILAYERED SUBSTRATE INTERDIGITAL CAPACITORS

      IEEE transactions on microwave theory and techniques
    71. ZIMMERMAN M; BORNSTEIN R; MARTINSSON T
      UTILIZATION OF DENTAL SERVICES IN REFUGEES IN SWEDEN 1975-1985

      Community dentistry and oral epidemiology
    72. MARTINSSON T; SJOBERG RM; HEDBORG F; KOGNER P
      DELETION OF CHROMOSOME 1P LOCI AND MICROSATELLITE INSTABILITY IN NEUROBLASTOMAS ANALYZED WITH SHORT-TANDEM REPEAT POLYMORPHISMS

      Cancer research
    73. SWANBECK G; INEROT A; MARTINSSON T; WAHLSTROM J; ENERBACK C; ENLUND F; YHR M
      AGE AT ONSET AND DIFFERENT TYPES OF PSORIASIS

      British journal of dermatology
    74. VUJIC M; HALLSTENSSON K; WAHLSTROM J; LUNDBERG A; LANGMAACK C; MARTINSSON T
      LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME TO CHROMOSOME REGION 3P21.1-14.1 IN THE PROXIMITY OF, BUT DISTINCT FROM, THE COL7A1 LOCUS

      American journal of human genetics
    75. MARTINSSON T; VUJIC M; HALLSTENSSON K; LUNDBERG A; LANGMAACK C; WAHLSTROM J
      LINKAGE OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME (LAR1) TO CHROMOSOME 3P-MARKERS

      American journal of human genetics
    76. KULLMAN L; MARTINSSON T; ZIMMERMAN M; WELANDER U
      COMPUTERIZED MEASUREMENTS OF THE LOWER 3RD MOLAR RELATED TO CHRONOLOGICAL AGE IN YOUNG-ADULTS

      Acta Odontologica Scandinavica
    77. MARTINSSON T; BJURSELL C; STIBLER H; KRISTIANSSON B; SKOVBY F; JAEKEN J; BLENNOW G; STROMME P; HANEFELD F; WAHLSTROM J
      LINKAGE OF A LOCUS FOR CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1) TO CHROMOSOME 16P, AND LINKAGE DISEQUILIBRIUM TO MICROSATELLITE MARKER D16S406

      Human molecular genetics
    78. RUNMARKER B; MARTINSSON T; WAHLSTROM J; ANDERSEN O
      HLA AND PROGNOSIS IN MULTIPLE-SCLEROSIS

      Journal of neurology
    79. BARR CL; KENNEDY JL; PAKSTIS AJ; WETTERBERG L; SJOGREN B; BIERUT L; WADELIUS C; WAHLSTROM J; MARTINSSON T; GIUFFRA L; GELERNTER J; HALLMAYER J; MOISES HW; KURTH J; CAVALLISFORZA LL; KIDD KK
      PROGRESS IN A GENOME SCAN FOR LINKAGE IN SCHIZOPHRENIA IN A LARGE SWEDISH KINDRED

      American journal of medical genetics
    80. SWANBECK G; INEROT A; MARTINSSON T; WAHLSTROM J; ENERBACK C; ENLUND F; YHR M
      GENETIC HETEROGENIETY IN PSORIASIS-VULGARIS BASED ON LINKAGE ANALYSISOF A LARGE FAMILY MATERIAL

      Journal of investigative dermatology
    81. OLDFORS A; MARTINSSON T; TESSIN I; WAHLSTROM J; WANG S
      DUCHENNE MUSCULAR-DYSTROPHY AND SPINAL MUSCULAR-ATROPHY TYPE-I SEGREGATING IN THE SAME FAMILY

      Clinical genetics
    82. SWANBECK G; INEROT A; MARTINSSON T; WAHLSTROM J
      A POPULATION GENETIC-STUDY OF PSORIASIS

      British journal of dermatology
    83. OLDFORS A; ERIKSSON BO; KYLLERMAN M; MARTINSSON T; WAHLSTROM J
      DILATED CARDIOMYOPATHY AND THE DYSTROPHIN GENE - AN ILLUSTRATED REVIEW

      British Heart Journal
    84. SWANBECK G; INEROT A; MARTINSSON T; WAHLSTROM J
      A POPULATION GENETIC-STUDY OF PSORIASIS

      Acta dermato-venereologica
    85. MARTINSSON T; VUJIC M; TOMKINSON B
      LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II GENE (TPP2) TO 13Q32-Q33 BY NONRADIOACTIVE IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRIDS

      Genomics
    86. DAHL N; GRANDELL U; MARTINSSON T; ALLEN M; JOHANSSON L; STOLPE L; GYLLENSTEN U; HJELTE L; KOLLBERG H; STRANDVIK B; WAHLSTROM J; ANVRET M
      FREQUENCY OF 4 CYSTIC-FIBROSIS MUTATIONS IN A SWEDISH POPULATION

      Acta paediatrica
    87. FOWLER CJ; MARTINSSON T; BRANNSTROM G
      SPECIFIC BINDING OF [H-3] [SAR(9),MET(O2)11]-SUBSTANCE-P TO TISSUE-CULTURE PLATES IS FOUND WHEN SUBSTANCE-P IS USED TO DEFINE NONSPECIFIC-BINDING

      Methods and findings in experimental and clinical pharmacology
    88. ZIMMERMAN M; BORNSTEIN R; MARTINSSON T
      SIMPLIFIED PREVENTIVE DENTISTRY PROGRAM FOR CHILEAN REFUGEES - EFFECTIVENESS OF ONE VERSUS 2 INSTRUCTIONAL SESSIONS

      Community dentistry and oral epidemiology
    89. UVEBRANT P; BJORCK E; CONRADI N; HOKEGARD KH; MARTINSSON T; WAHLSTROM J
      SUCCESSFUL DNA-BASED PRENATAL EXCLUSION OF JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS

      Prenatal diagnosis
    90. MARTINSSON T; HAEGERSTRAND A; DALSGAARD CJ
      ROPIVACAINE AND LIDOCAINE INHIBIT PROLIFERATION OF NONTRANSFORMED CULTURED ADULT HUMAN FIBROBLASTS, ENDOTHELIAL-CELLS AND KERATINOCYTES

      Agents and actions
    91. MARTINSSON T; FOWLER CJ
      LOCAL-ANESTHETICS DO NOT AFFECT PROTEIN-KINASE-C FUNCTION IN INTACT NEUROBLASTOMA-CELLS

      Life sciences
    92. WAHLSTROM J; SWANBECK G; INEROT A; MARTINSSON T
      POPULATION GENETIC-ANALYSIS OF PSORIASIS

      American journal of human genetics
    93. MARTINSSON T; VUJIC M; TOMKINSON B
      CHROMOSOMAL LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II (TPP2)GENE TO 13Q32-33

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/01/21 alle ore 20:15:28