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 'LARGE PEDIGREE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 20 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. 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
    2. Deschauer, M; Muller, T; Wieser, T; Schulte-Mattler, W; Kornhuber, M; Zierz, S
      Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation

      ARCHIVES OF NEUROLOGY
    3. Balestri, P; Grosso, S
      Endocrine disorders in two sisters affected by MELAS syndrome

      JOURNAL OF CHILD NEUROLOGY
    4. Drouet, A; Guilloton, L; Godinot, C; Rochet, D; Ribot, C; Carrier, H
      Complicated diabetes-deafness syndrome or association with a MELAS syndrome, in a patient harboring the mitochondrial DNA mutation at position 3243?

      REVUE NEUROLOGIQUE
    5. Damore, ME; Speiser, PW; Slonim, AE; New, MI; Shanske, S; Xia, WL; Santorelli, FM; DiMauro, S
      Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: Patient report and literature review

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    6. Lichter, DG; Dmochowski, J; Jackson, LA; Trinidad, KS
      Influence of family history on clinical expression of Tourette's syndrome

      NEUROLOGY
    7. Hedera, P; Rainier, S; Alvarado, D; Zhao, XP; Williamson, J; Otterud, B; Leppert, M; Fink, JK
      Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q

      AMERICAN JOURNAL OF HUMAN GENETICS
    8. ONISHI H; HANIHARA T; SUGIYAMA N; KAWANISHI C; ISEKI E; MARUYAMA Y; YAMADA Y; KOSAKA K; YAGISHITA S; SEKIHARA H; SATOH S
      PANCREATIC EXOCRINE DYSFUNCTION ASSOCIATED WITH MITOCHONDRIAL TRNA(LEU(UUR)) MUTATION

      Journal of Medical Genetics
    9. DAMIAN MS; HERTEL A; SEIBEL P; REICHMANN H; BACHMANN G; SCHACHENMAYR W; HOER G; DORNDORF W
      FOLLOW-UP IN CARRIERS OF THE MELAS MUTATION WITHOUT STROKES

      European neurology
    10. SIMONIC I; GERICKE GS; OTT J; WEBER JL
      IDENTIFICATION OF GENETIC-MARKERS ASSOCIATED WITH GILLES-DE-LA-TOURETTE-SYNDROME IN AN AFRIKANER POPULATION

      American journal of human genetics
    11. BREDIE SJH; VANDRONGELEN J; KIEMENEY LA; DEMACKER PNM; BEATY TH; STALENHOEF AFH
      SEGREGATION ANALYSIS OF PLASMA APOLIPOPROTEIN-B LEVELS IN FAMILIAL COMBINED HYPERLIPIDEMIA

      Arteriosclerosis, thrombosis, and vascular biology
    12. TANNER CM; GOLDMAN SM
      EPIDEMIOLOGY OF TOURETTE-SYNDROME

      Neurologic clinics
    13. LIZCANOGIL LA; GARCIACRUZ D; BERNALBELTRAN MDP; HERNANDEZ A
      ASSOCIATION OF LATE-ONSET SPASTIC PARAPARESIS AND DEMENTIA - PROBABLYAN AUTOSOMAL-DOMINANT FORM OF COMPLICATED PARAPLEGIA

      American journal of medical genetics
    14. VILARINHO L; SANTORELLI FM; ROSAS MJ; TAVARES C; MELOPIRES M; DIMAURO S
      THE MITOCHONDRIAL A3243G MUTATION PRESENTING AS SEVERE CARDIOMYOPATHY

      Journal of Medical Genetics
    15. STALEY D; WAND R; SHADY G
      TOURETTE DISORDER - A CROSS-CULTURAL REVIEW

      Comprehensive psychiatry
    16. SPEER MC; KINGSTON HM; BOUSTANY RMN; GASKELL PC; ROBINSON LC; LENNON F; WOLPERT CM; YAMAOKA LH; KAHLER SG; HOGAN EL; CUMMING WJK; PERICAKVANCE MA
      CONFIRMATION OF LOCUS HETEROGENEITY IN THE PURE FORM OF FAMILIAL SPASTIC PARAPLEGIA

      American journal of medical genetics
    17. SRINIVASAN SR; BERENSON GS
      SERUM APOLIPOPROTEIN-A-I AND APOLIPOPROTEIN-B AS MARKERS OF CORONARY-ARTERY-DISEASE RISK IN EARLY-LIFE - THE BOGALUSA HEART-STUDY

      Clinical chemistry
    18. CULLEN P; FARREN B; SCOTT J; FARRALL M
      COMPLEX SEGREGATION ANALYSIS PROVIDES EVIDENCE FOR A MAJOR GENE ACTING ON SERUM TRIGLYCERIDE LEVELS IN 55 BRITISH FAMILIES WITH FAMILIAL COMBINED HYPERLIPIDEMIA

      Arteriosclerosis and thrombosis
    19. BARONCOHEN S; CROSS P; CROWSON M; ROBERTSON M
      CAN CHILDREN WITH GILLES-DE-LA-TOURETTE-SYNDROME EDIT THEIR INTENTIONS

      Psychological medicine
    20. ROBERTSON MM
      GILLES-DE-LA-TOURETTE SYNDROME - AN UPDATE

      Journal of child psychology and psychiatry and allied disciplines


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 02:16:25