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 ' HOLMGREN G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 99 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Mardh, CK; Backman, B; Simmons, D; Golovleva, I; Gu, TT; Holmgren, G; MacDougall, M; Forsman-Semb, K
      Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients

      EUROPEAN JOURNAL OF ORAL SCIENCES
    2. Nordgren, A; Farnebo, F; Johansson, B; Holmgren, G; Forestier, E; Larsson, C; Soderhall, S; Nordenskjold, M; Blennow, E
      Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping

      EUROPEAN JOURNAL OF HAEMATOLOGY
    3. Suhr, OB; Lang, K; Wikstrom, L; Anan, I; Ando, Y; El-Salhy, M; Holmgren, G; Tashima, K
      Scavenger treatment of free radical injury in familial amyloidotic polyneuropathy: a study on Swedish transplanted and non-transplanted patients

      SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
    4. Holmgren, G
      Reply to: Comparative evaluation of the Misgav Ladach cesarean section with two traditional techniques. The first four years' experience

      ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
    5. Janunger, T; Anan, I; Holmgren, G; Lovheim, O; Ohlsson, PI; Suhr, OB; Tashima, K
      Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    6. Jonasson, J; Juvonen, V; Sistonen, P; Ignatius, J; Johansson, D; Bjorck, EJ; Wahlstrom, J; Melberg, A; Holmgren, G; Forsgren, L; Holmberg, M
      Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Klein, C; Gurvich, N; Sena-Esteves, M; Bressman, S; Brin, MF; Ebersole, BJ; Fink, S; Forsgren, L; Friedman, J; Grimes, D; Holmgren, G; Kyllerman, M; Lang, AE; de Leon, D; Leung, J; Prioleau, C; Raymond, D; Sanner, G; Saunders-Pullman, R; Vieregge, P; Wahlstrom, J; Breakefield, XO; Kramer, PL; Ozelius, LJ; Sealfon, SC
      Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia

      ANNALS OF NEUROLOGY
    8. Mambule, C; Ando, Y; Anan, I; Holmgren, G; Sandgren, O; Stigbrandt, T; Tashima, K; Suhr, OB
      Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol

      BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
    9. Halfvarsson, J; Heijne, N; Ljungman, P; Ham, MN; Holmgren, G; Tomson, G
      Knowing when but not how! - Mothers' perceptions and use of antibiotics ina rural area of Viet Nam

      TROPICAL DOCTOR
    10. Holmgren, G
      Burns and skin grafting

      TROPICAL DOCTOR
    11. Klein, C; Schilling, K; Saunders-Pullman, RJ; Garrels, J; Breakefield, XO; Brin, MF; deLeon, D; Doheny, D; Fahn, S; Fink, JS; Forsgren, L; Friedman, J; Frucht, S; Harris, J; Holmgren, G; Kis, B; Kurlan, R; Kyllerman, M; Lang, AE; Leung, J; Raymond, D; Robishaw, JD; Sanner, G; Schwinger, E; Tabamo, RE; Tagliati, M; Vieregge, P; Wahlstrom, J; Wendt, KJ; Kramer, PL; Bressman, SB; Ozelius, LJ
      A major locus for myoclonus-dystonia maps to chromosome 7q in eight families

      AMERICAN JOURNAL OF HUMAN GENETICS
    12. Holmgren, G; Sjoholm, L; Stark, M
      Modifications to the Misgav Ladach technique for cesarean section - Reply from the authors

      ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
    13. Tashima, K; Suhr, OB; Ando, Y; Holmgren, G; Yamashita, T; Obayashi, K; Terazaki, H; Uchino, M
      Gastrointestinal dysfunction in familial amyloidotic polyneuropathy (ATTR Val30Met) - comparison of Swedish and Japanese patients

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    14. Suhr, OB; Holmgren, G
      Untitled

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    15. Burstedt, MSI; Sandgren, O; Holmgren, G; Forsman-Semb, K
      Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    16. Lendoire, JC; Trigo, P; Aziz, H; Romero, MC; Inventarza, O; Ando, Y; Tashima, K; Ohlsson, PI; Cederquist, K; Holmgren, G; Suhr, OB
      Variant transthyretin (TTR) amyloidosis in Argentina. Detection of the trait by electrospray ionization mass spectrometry of lyophilized TTR immunoprecipitate

      SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
    17. Holmgren, G; Sjoholm, L; Stark, M
      The Misgav Ladach method for cesarean section: method description

      ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
    18. STASIEWICZ K; HOLMGREN G; ZANETTI L
      DENSITY DEPLETIONS AND CURRENT SINGULARITIES OBSERVED BY FREJA

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    19. PETRUKHIN K; KOISTI MJ; BAKALL B; LI W; XIE GC; MARKNELL T; SANDGREN O; FORSMAN K; HOLMGREN G; ANDREASSON S; VUJIC M; BERGEN AAB; MCGARTYDUGAN V; FIGUEROA D; AUSTIN CP; METZKER ML; CASKEY CT; WADELIUS C
      IDENTIFICATION OF THE GENE RESPONSIBLE FOR BEST MACULAR DYSTROPHY

      Nature genetics
    20. SOUSA A; COELHO T; LOBATO L; BARROS J; FERREIRA C; ANDERSSON R; DRUGGE U; SANDGREN O; HOLMGREN G; SEQUEIROS J
      FAMILIAL AMYLOID POLYNEUROPATHY (FAP-MET30) IN PORTUGAL AND SWEDEN - PHENOTYPIC VARIABILITY AND DEPARTURES FROM MENDELIAN INHERITANCE

      European journal of human genetics
    21. JOHANSSON J; FORSGREN L; SANDGREN O; BRICE A; HOLMGREN G; HOLMBERG M
      EXPANDED CAG REPEATS IN SWEDISH SPINOCEREBELLAR ATAXIA TYPE-7 (SCA7) PATIENTS - EFFECT OF CAG REPEAT LENGTH ON THE CLINICAL MANIFESTATION

      Human molecular genetics
    22. ANDO Y; ANAN I; SUHR O; HOLMGREN G; COSTA PMP
      DETECTION OF A VARIANT PROTEIN IN HAIR - NEW DIAGNOSTIC METHOD IN PORTUGUESE TYPE FAMILIAL AMYLOID POLYNEUROPATHY

      BMJ. British medical journal
    23. Forestier, E; Holmgren, G; Roos, G
      Flow cytometric DNA index and karyotype in childhood lymphoblastic leukemia

      ANALYTICAL CELLULAR PATHOLOGY
    24. ANDO Y; SUHR O; YAMASHITA T; OHLSSON PI; HOLMGREN G; OBAYASHI K; TERAZAKI H; MAMBULE C; UCHINO M; ANDO M
      DETECTION OF DIFFERENT FORMS OF VARIANT TRANSTHYRETIN (MET30) IN CEREBROSPINAL-FLUID (VOL 238, PG 123, 1997)

      Neuroscience letters
    25. SUHR OB; HOLMGREN G; ANDO Y
      IMPROVEMENT IN THE POLYNEUROPATHY ASSOCIATED WITH FAMILIAL AMYLOID POLYNEUROPATHY AFTER LIVER-TRANSPLANTATION

      Neurology
    26. SUHR O; ANDO Y; OHLSSON PI; OLOFSSON A; ANDERSSON K; LUNDGREN E; ANDO M; HOLMGREN G
      INVESTIGATION INTO THIOL CONJUGATION OF TRANSTHYRETIN IN HEREDITARY TRANSTHYRETIN AMYLOIDOSIS

      European journal of clinical investigation
    27. WAHLIN A; SANDSTROM H; LIND L; HOLMGREN G; SANDGREN O; WICKRAMASINGHE S
      DEALING WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA, TYPE-III, AND ITS CANDIDATE GENE

      British Journal of Haematology
    28. PEKKARINEN P; HOVATTA I; HAKOLA P; JARVI O; KESTILA M; LENKKERI U; ADOLFSSON R; HOLMGREN G; NYLANDER PO; TRANEBJAERG L; TERWILLIGER JD; LONNQVIST J; PELTONEN L
      ASSIGNMENT OF THE LOCUS FOR PLO-SL, A FRONTAL-LOBE DEMENTIA WITH BONE-CYSTS, TO 19Q13

      American journal of human genetics
    29. ERIKSSON AI; MALKKI A; DOVNER PO; BOSTROM R; HOLMGREN G; HOLBACK B
      A STATISTICAL-SURVEY OF AURORAL SOLITARY WAVES AND WEAK DOUBLE-LAYERS.2. MEASUREMENT ACCURACY AND AMBIENT PLASMA-DENSITY

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    30. HOLMGREN G; ANDO Y; WIKSTROM L; RYDH A; SUHR O
      DISCORDANT SYMPTOMS IN MONOZYGOTIC TWINS WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY (FAP) (TTR-MET-30)

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    31. NELIS E; HOLMBERG B; ADOLFSSON R; HOLMGREN G; VANBROECKHOVEN C
      PMP22 THR(118)MET - RECESSIVE CMT1 MUTATION OR POLYMORPHISM

      Nature genetics
    32. HOLMGREN G
      REES,HARRY - OBITUARY

      BMJ. British medical journal
    33. MACDOUGALL M; DUPONT BR; SIMMONS D; REUS B; KREBSBACH P; KARRMAN C; HOLMGREN G; LEACH RJ; FORSMAN K
      AMELOBLASTIN GENE (AMBN) MAPS WITHIN THE CRITICAL REGION FOR AUTOSOMAL-DOMINANT AMELOGENESIS IMPERFECTA AT CHROMOSOME 4Q21

      Genomics
    34. KARRMAN C; BACKMAN B; DIXON M; HOLMGREN G; FORSMAN K
      MAPPING OF THE LOCUS FOR AUTOSOMAL-DOMINANT - AMELOGENESIS IMPERFECTA(AIH2) TO A 4-MB YAC CONTIG ON CHROMOSOME 4Q11-Q21

      Genomics
    35. GRAFF C; ERIKSSON A; FORSMAN K; SANDGREN O; HOLMGREN G; WADELIUS C
      REFINED GENETIC LOCALIZATION OF THE BEST-DISEASE GENE IN 11Q13 AND PHYSICAL MAPPING OF LINKED MARKERS ON RADIATION HYBRIDS

      Human genetics
    36. ANDO Y; SUHR O; YAMASHITA T; OHLSSON PI; HOLMGREN G; OBAYASHI K; TERAZAKI H; MAMBULE C; UCHINO M; ANDO M
      DETECTION OF DIFFERENT FORMS OF VARIANT TRANSTHYRETIN (MET30) IN CEREBROSPINAL-FLUID

      Neuroscience letters
    37. SILLEN A; HOLMGREN G; WADELIUS C
      FIRST PRENATAL-DIAGNOSIS BY MUTATION ANALYSIS IN A FAMILY WITH SJOGREN-LARSSON-SYNDROME

      Prenatal diagnosis
    38. PEKKARINEN P; HOVATTA I; JARVI O; LONNQVIST J; ADOLFSSON R; NYLANDER PO; HOLMGREN G; TRANEBJAERG L; HAKOLA P; PELTONEN L
      GENOME SCAN REVEALS A LOCUS FOR A PREFRONTAL DEMENTIA WITH BONE-CYSTSON CHROMOSOME-19

      American journal of medical genetics
    39. PEDERSEN A; CORNILLEAUWEHRLIN N; DELAPORTE B; ROUX A; BOUABDELLAH A; DECREAU PME; LEFEUVRE F; SENE FX; GURNETT D; HUFF R; GUSTAFSSON G; HOLMGREN G; WOOLLISCROFT L; ALLEYNE HS; THOMPSON JA; DAVIES PHN
      THE WAVE EXPERIMENT CONSORTIUM (WEC)

      Space science reviews
    40. GUSTAFSSON G; BOSTROM R; HOLBACK B; HOLMGREN G; LUNDGREN A; STASIEWICZ K; AHLEN L; MOZER FS; PANKOW D; HARVEY P; BERG P; ULRICH R; PEDERSEN A; SCHMIDT R; BUTLER A; FRANSEN AWC; KLINGE D; THOMSEN M; FALTHAMMAR CG; LINDQVIST PA; CHRISTENSON S; HOLTET J; LYBEKK B; STEN TA; TANSKANEN P; LAPPALAINEN K; WYGANT J
      THE ELECTRIC-FIELD AND WAVE EXPERIMENT FOR THE CLUSTER MISSION

      Space science reviews
    41. WOOLLISCROFT LJC; ALLEYNE HS; DUNFORD CM; SUMNER A; THOMPSON JA; WALKER SN; YEARBY KH; BUCKLEY A; CHAPMAN S; GOUGH MP; BALIKHIN MA; BURGESS D; CORNILLEAUWEHRLIN N; ROUX A; DECREAU PME; KRASNOSELSKIKH VV; LEFEUVRE F; PARROT M; EGELAND A; GEDALIN M; GURNETT D; GUSTAFSSON G; HOLMGREN G; HARVEY CC; HORNE R; IVERSEN IB; KOFMAN W; KOONS HC; LABELLE JA; MOZER F; REZNIKOV A
      THE DIGITAL WAVE-PROCESSING EXPERIMENT ON CLUSTER

      Space science reviews
    42. SIMMONS D; DUPONT B; LEACH RJ; KARRMAN C; BACKMAN B; HOLMGREN G; FORSMAN K; MACDOUGALL M
      AMELOBLASTIN - CANDIDATE GENE FOR THE AUTOSOMAL-DOMINANT AMELOGENESISIMPERFECTA (ALH2)

      Journal of dental research
    43. RANLOV I; ANDO Y; OHLSSON PI; HOLMGREN G; RANLOV PJ; SUHR OB
      RAPID SCREENING FOR AMYLOID-RELATED VARIANT FORMS OF TRANSTHYRETIN ISPOSSIBLE BY ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY

      European journal of clinical investigation
    44. SANDSTROM H; WAHLIN A; ERIKSSON M; HOLMGREN G; LIND L; SANDGREN O
      ANGIOID STREAKS ARE PART OF A FAMILIAL SYNDROME OF DYSERYTHROPOIETIC ANEMIA (CDA-III)

      British Journal of Haematology
    45. ANDO Y; NYHLIN N; SUHR O; HOLMGREN G; UCHIDA K; ELSAHLY M; YAMASHITA T; TERASAKI H; NAKAMURA M; UCHINO M; ANDO M
      OXIDATIVE STRESS IS FOUND IN AMYLOID DEPOSITS IN SYSTEMIC AMYLOIDOSIS

      Biochemical and biophysical research communications
    46. PEKKARINEN P; HOVATTA I; HAKOLA P; JARVI O; LONNQVIST J; ADOLFSSON R; NYLANDER PO; HOLMGREN G; TRANEBJAERG L; PELTONEN L
      GENOME SCAN REVEALS A LOCUS FOR PLO-SL, A PREFRONTAL DEMENTIA WITH BONE-CYSTS ON CHROMOSOME-19

      American journal of human genetics
    47. LIND LK; LUNDSTROM A; HOLMGREN G
      REFINED MAPPING OF THE LOCUS FOR PALMOPLANTAR KERATODERMA TYPE BOTHNIA

      American journal of human genetics
    48. ELIASSON L; ANDRE M; LUNDIN R; POTTELETTE R; MARKLUND G; HOLMGREN G
      OBSERVATIONS OF ELECTRON CONICS BY THE VIKING SATELLITE

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    49. ALVES IL; JACOBSON DR; TORRES MF; HOLMGREN G; BUXBAUM J; SARAIVA MJM
      TRANSTHYRETIN SER6 AS A NEUTRAL POLYMORPHISM IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    50. WIKSTROM L; BJERLE P; BOMAN K; HOLMGREN G; STEEN L
      L-THREO-DOPS TREATMENT OF ORTHOSTATIC HYPOTENSION IN SWEDISH PATIENTSWITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY (TTR-MET(30))

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    51. LINDBLAD K; SAVONTAUS ML; STEVANIN G; HOLMBERG M; DIGRE K; ZANDER C; EHRSSON H; DAVID G; BENOMAR A; NIKOSKELAINEN E; TROTTIER Y; HOLMGREN G; PTACEK LJ; ANTTINEN A; BRICE A; SCHALLING M
      AN EXPANDED CAG REPEAT SEQUENCE IN SPINOCEREBELLAR ATAXIA TYPE-7

      PCR methods and applications
    52. HOLMGREN G; SJOHOLM L
      THE MISGAV-LADACH METHOD OF CESAREAN-SECTION - EVOLVED BY COHEN,JOEL AND STARK,MICHAEL IN JERUSALEM

      Tropical doctor
    53. FORSGREN L; LIBELIUS R; HOLMBERG M; VONDOBELN U; WIBOM R; HEIJBEL J; SANDGREN O; HOLMGREN G
      MUSCLE MORPHOLOGY AND MITOCHONDRIAL INVESTIGATIONS OF A FAMILY WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA AND RETINAL DEGENERATION MAPPED TOCHROMOSOME 3P12-P21.1

      Journal of the neurological sciences
    54. NYLANDER PO; DRUGGE U; HOLMGREN G; ADOLFSSON R
      POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY (PLO-SL) - A GENEALOGICAL STUDY OF SWEDISH FAMILIES OF PROBABLE FINNISH BACKGROUND

      Clinical genetics
    55. BLOMQUIST HK; DAHL N; GUSTAFSSON L; HELLERUD C; HOLME E; HOLMGREN G; MATSSON L; VONZWEIGBERGK M
      GLYCEROL KINASE-DEFICIENCY IN 2 BROTHERS WITH AND WITHOUT CLINICAL MANIFESTATIONS

      Clinical genetics
    56. ANDO Y; OHLSSON PI; SUHR O; NYHLIN N; YAMASHITA T; HOLMGREN G; DANIELSSON A; SANDGREN O; UCHINO M; ANDO M
      A NEW SIMPLE AND RAPID SCREENING METHOD FOR VARIANT TRANSTHYRETIN-RELATED AMYLOIDOSIS

      Biochemical and biophysical research communications
    57. KARRMAN C; BACKMAN B; HOLMGREN G; FORSMAN K
      GENETIC-HETEROGENEITY OF AUTOSOMAL-DOMINANT AMELOGENESIS IMPERFECTA DEMONSTRATED BY ITS EXCLUSION FROM THE AIH2 REGION ON HUMAN-CHROMOSOME 4Q

      Archives of oral biology
    58. LOVAT LB; BOOTH SE; BOOTH DR; MADHOO S; HOLMGREN G; HAWKINS PN; SOUTAR AK; PEPYS MB
      APOLIPOPROTEIN E4 GENOTYPE IS NOT A RISK FACTOR FOR SYSTEMIC AA AMYLOIDOSIS OR FAMILIAL AMYLOID POLYNEUROPATHY

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    59. SUHR O; HOLMGREN G
      DIFFICULTIES IN CLINICAL-DIAGNOSIS AND PREDICTION OF OUTCOME IN PATIENTS WITH THE TRANSTHYRETIN MET-30 MUTATION - REPORT OF 2 CASES

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    60. HARDELL L; HOLMGREN G; STEEN L; FREDRIKSON M; AXELSON O
      OCCUPATIONAL AND OTHER RISK-FACTORS FOR CLINICALLY OVERT FAMILIAL AMYLOID POLYNEUROPATHY

      Epidemiology
    61. HOLMBERG M; JOHANSSON J; FORSGREN L; HEIJBEL J; SANDGREN O; HOLMGREN G
      LOCALIZATION OF AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA ASSOCIATED WITH RETINAL DEGENERATION AND ANTICIPATION TO CHROMOSOME 3P12-P21.1

      Human molecular genetics
    62. LIND L; SANDSTROM H; WAHLIN A; ERIKSSON M; NILSSONSOJKA B; SIKSTROM C; HOLMGREN G
      LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-III, CDAN3, TO CHROMOSOME 15Q21 - Q25

      Human molecular genetics
    63. BALCIUNIENE J; JOHANSSON K; SANDGREN O; WACHTMEISTER L; HOLMGREN G; FORSMAN K
      A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE CONE DYSTROPHY (CORD5) MAPSTO CHROMOSOME 17P12-P13

      Genomics
    64. ERIKSON A; FORSBERG H; DRUGGE U; HOLMGREN G
      OUTCOME OF PREGNANCY IN WOMEN WITH MYOTONIC-DYSTROPHY AND ANALYSIS OFCTG GENE EXPANSION

      Acta paediatrica
    65. ALMEIDA MR; AOYAMAOISHI N; SAKAKI Y; HOLMGREN G; ULF D; FERLINI A; SALVI F; MUNARQUES M; BENSON MD; SKINNER M; COSTA PP; SARAIVA MJ
      HAPLOTYPE ANALYSIS OF COMMON TRANSTHYRETIN MUTATIONS

      Human genetics
    66. ERICZON BG; SUHR O; BROOME U; HOLMGREN G; DURAJ F; ELEBORG L; WIKSTROM L; NORDEN G; FRIMAN S; GROTH CG
      LIVER-TRANSPLANT HALTS THE PROGRESS OF FAMILIAL AMYLOIDOTIC POLYNEUROPATHY

      Transplantation proceedings
    67. SUHR OB; HOLMGREN G; STEEN L; WIKSTROM L; NORDEN G; FRIMAN S; DURAJ FF; GROTH CG; ERICZON BG
      LIVER-TRANSPLANTATION IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY - FOLLOW-UP OF THE FIRST 20 SWEDISH PATIENTS

      Transplantation
    68. HOLMGREN G; OZELIUS L; FORSGREN L; ALMAY BGL; HOLMBERG M; KRAMER P; FAHN S; BREAKEFIELD XO
      ADULT-ONSET IDIOPATHIC TORSION DYSTONIA IS EXCLUDED FROM THE DYT1 REGION (9Q34) IN A SWEDISH FAMILY

      Journal of Neurology, Neurosurgery and Psychiatry
    69. DRUGGE U; HOLMBERG M; HOLMGREN G; ALMAY BGL; LINDERHOLM H
      HEREDITARY MYOPATHY WITH LACTIC-ACIDOSIS, SUCCINATE-DEHYDROGENASE ANDACONITASE DEFICIENCY IN NORTHERN SWEDEN - A GENEALOGICAL STUDY

      Journal of Medical Genetics
    70. FORSMAN K; KARRMAN C; BACKMAN B; DIXON M; HOLMGREN G
      REFINED MAPPING OF THE AMELOGENESIS IMPERFECTA LOCUS ON 4Q

      American journal of human genetics
    71. WADELIUS C; GRAFF C; FORSMAN K; ERIKSSON A; SANDGREN O; WEISSENBACH J; HOLMGREN G; GUSTAVSON KH
      HIGH-RESOLUTION MEIOTIC MAPPING OF THE BESTS MACULAR DYSTROPHY - THE GENE IS FLANKED BY UGB AND FCERI

      American journal of human genetics
    72. LIND L; SANDSTROM H; WAHLIN A; ERIKSSON M; HOLMGREN G
      REFINED MAPPING OF THE LOCUS FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-III (CDA-III) TO CHROMOSOME 15Q22.1

      American journal of human genetics
    73. MALKKI A; ERIKSSON AI; DOVNER PQ; BOSTROM R; HOLBACK B; HOLMGREN G; KOSKINEN HEJ
      A STATISTICAL-SURVEY OF AURORAL SOLITARY WAVES AND WEAK DOUBLE-LAYERS, 1, OCCURRENCE AND NET VOLTAGE (VOL 98, PG 15521, 1993)

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    74. STEEN L; HOLMGREN G; SUHR O; WIKSTROM L; GROTH CG; ERICZON BG
      WORLDWIDE SURVEY OF LIVER-TRANSPLANTATION IN PATIENTS WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    75. FORSMAN K; LIND L; BACKMAN B; WESTERMARK E; HOLMGREN G
      LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT AMELOGENESIS IMPERFECTA(ADAI) TO CHROMOSOME 4Q

      Human molecular genetics
    76. LIND L; LUNDSTROM A; HOFER PA; HOLMGREN G
      THE GENE FOR DIFFUSE PALMOPLANTAR KERATODERMA OF THE TYPE FOUND IN NORTHERN SWEDEN IS LOCALIZED TO CHROMOSOME 12Q11-Q13

      Human molecular genetics
    77. SUHR O; DANIELSSON A; HOLMGREN G; STEEN L
      MALNUTRITION AND GASTROINTESTINAL DYSFUNCTION AS PROGNOSTIC FACTORS FOR SURVIVAL IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY

      Journal of internal medicine
    78. GRAFF C; FORSMAN K; LARSSON C; NORDSTROM S; LIND L; JOHANSSON K; SANDGREN O; WEISSENBACH J; HOLMGREN G; GUSTAVSON KH; WADELIUS C
      FINE MAPPING OF BESTS MACULAR DYSTROPHY LOCALIZES THE GENE IN CLOSE PROXIMITY TO BUT DISTINCT FROM THE D11S480 ROM1 LOCI/

      Genomics
    79. WAHLUND JE; LOUARN P; CHUST T; DEFERAUDY H; ROUX A; HOLBACK B; DOVNER PO; HOLMGREN G
      ON ION-ACOUSTIC TURBULENCE AND THE NONLINEAR EVOLUTION OF KINETIC ALFVEN WAVES IN AURORA

      Geophysical research letters
    80. STASIEWICZ K; GUSTAFSSON G; HOLMGREN G; HOLBACK B; ELIASSON L; KINTNER PM; ZANETTI L
      WAVE ENVIRONMENT INSIDE AN INVERTED-V ELECTRON EVENT OBSERVED BY FREJA

      Geophysical research letters
    81. ERIKSSON AI; HOLBACK B; DOVNER PO; BOSTROM R; HOLMGREN G; ANDRE M; ELIASSON L; KINTNER PM
      FREJA OBSERVATIONS OF CORRELATED SMALL-SCALE DENSITY DEPLETIONS AND ENHANCED LOWER-HYBRID WAVES

      Geophysical research letters
    82. LOUARN P; WAHLUND JE; CHUST T; DEFERAUDY H; ROUX A; HOLBACK B; DOVNER PO; ERIKSSON AI; HOLMGREN G
      OBSERVATION OF KINETIC ALFVEN WAVES BY THE FREJA SPACECRAFT

      Geophysical research letters
    83. BINZER M; FORSGREN L; HOLMGREN G; DRUGGE U; FREDRIKSON S
      FAMILIAL CLUSTERING OF MULTIPLE-SCLEROSIS IN A NORTHERN SWEDISH RURALDISTRICT

      Journal of Neurology, Neurosurgery and Psychiatry
    84. HOLMBERG BH; HOLMGREN G; NELIS E; VANBROECKHOVEN C; WESTERBERG B
      CHARCOT-MARIE-TOOTH DISEASE IN NORTHERN SWEDEN - PEDIGREE ANALYSIS AND THE PRESENCE OF THE DUPLICATION IN CHROMOSOME 17P11.2

      Journal of Medical Genetics
    85. HOLMGREN G; COSTA PMP; ANDERSSON C; ASPLUND K; STEEN L; BEEKMAN L; NYLANDER PO; TEIXEIRA A; SARAIVA MJM; COSTA PP
      GEOGRAPHICAL-DISTRIBUTION OF TTR MET(30) CARRIERS IN NORTHERN SWEDEN - DISCREPANCY BETWEEN CARRIER FREQUENCY AND PREVALENCE RATE

      Journal of Medical Genetics
    86. WAHLSTROM J; OZELIUS L; KRAMER P; KYLLERMAN M; SCHUBACK D; FORSGREN L; HOLMGREN G; DRUGGE U; SANNER G; FAHN S; BREAKEFIELD XO
      THE GENE FOR FAMILIAL DYSTONIA WITH MYOCLONIC JERKS RESPONSIVE TO ALCOHOL IS NOT LOCATED ON THE DISTAL END OF 9Q

      Clinical genetics
    87. KUCINSKAS V; JURGELEVICIUS V; CIMBALISTIENE L; HOLMGREN G
      DISTRIBUTIONS OF PHENYLALANINE-HYDROXYLASE MUTATIONS AND HAPLOTYPES IN LITHUANIAN PHENYLKETONURIA PATIENTS

      Human heredity
    88. MALKKI A; ERIKSSON AI; DOVNER PO; BOSTROM R; HOLBACK B; HOLMGREN G; KOSKINEN HEJ
      A STATISTICAL-SURVEY OF AURORAL SOLITARY WAVES AND WEAK DOUBLE-LAYERS.1. OCCURRENCE AND NET VOLTAGE

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    89. LEENDERS K; HARTVIG P; FORSGREN L; HOLMGREN G; ALMAY B; ECKERNAS SA; LUNDQVIST H; LANGSTROM B
      STRIATAL [C-11] N-METHYL-SPIPERONE BINDING IN PATIENTS WITH FOCAL DYSTONIA (TORTICOLLIS) USING POSITRON EMISSION TOMOGRAPHY

      Journal of neural transmission. Parkinson's disease and dementia section
    90. WAHLSTROM J; HOLMGREN G; ALBERTSSONWIKLAND K; TORNHAGE CJ
      SILVER-LIKE SYNDROME AND A SMALL DELETION ON CHROMOSOME-13

      Acta paediatrica
    91. KYLLERMAN M; SANNER G; FORSGREN L; HOLMGREN G; WAHLSTROM J
      EARLY-ONSET DYSTONIA DECREASING WITH DEVELOPMENT - CASE-REPORT OF 2 CHILDREN WITH FAMILIAL MYOCLONIC DYSTONIA

      Brain & development
    92. PETERS AM; HAWKINS PN; VIGUSHIN DM; RICHARDSON S; SEYMOUR A; HOLMGREN G; STEEN L; WOO P; HALL A; PEPYS MB
      REGRESSION OF AMYLOIDOSIS DEMONSTRATED BY SAP SCINTIGRAPHY

      The Journal of nuclear medicine
    93. HOLMGREN G; ERICZON BG; GROTH CG; STEEN L; SUHR O; ANDERSEN O; WALLIN BG; SEYMOUR A; RICHARDSON S; HAWKINS PN; PEPYS MB
      CLINICAL IMPROVEMENT AND AMYLOID REGRESSION AFTER LIVER-TRANSPLANTATION IN HEREDITARY TRANSTHYRETIN AMYLOIDOSIS

      Lancet
    94. DRUGGE U; ANDERSSON R; CHIZARI F; DANIELSSON M; HOLMGREN G; SANDGREN O; SOUSA A
      FAMILIAL AMYLOIDOTIC POLYNEUROPATHY IN SWEDEN - A PEDIGREE ANALYSIS

      Journal of Medical Genetics
    95. MALMGREN H; GUSTAVSON KH; HOLMGREN G; PETTERSSON U; DAHL N
      STRONG FOUNDER EFFECT FOR THE FRAGILE X-SYNDROME IN SWEDEN

      American journal of human genetics
    96. LIND L; SIKSTROM C; SANDSTROM H; WAHLIN A; ERIKSSON M; NILSSON B; HOLMGREN G
      THE LOCUS FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-III (CDA-III),ASSOCIATED WITH MONOCLONAL GAMMOPATHY AND MYELOMA, IS LOCALIZED ON CHROMOSOME-15Q21

      American journal of human genetics
    97. NYLANDER PO; LIND L; HOLMGREN G
      A LARGE SWEDISH FAMILY WITH PERIODIC BONE PAIN AND MIGRAINE

      American journal of human genetics
    98. WADELIUS C; GRAFF C; FORSMAN K; LIND L; WESTERMARK E; LARSSON C; SANDGREN O; GUSTAVSON KH; HOLMGREN G
      DETAILED MAPPING OF HEREDITARY VITTELIFORM MACULAR DYSTROPHY

      American journal of human genetics
    99. SOUSA A; ANDERSSON R; DRUGGE U; HOLMGREN G; SANDGREN O
      FAMILIAL AMYLOIDOTIC POLYNEUROPATHY IN SWEDEN - GEOGRAPHICAL-DISTRIBUTION, AGE-OF-ONSET, AND PREVALENCE

      Human heredity


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/08/20 alle ore 12:51:18