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La ricerca find articoli where authors phrase all words ' Pierpont, ME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 19 riferimenti
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    1. Hokanson, JS; Pierpont, ME; Hirsch, B; Moller, JH
      22q11.2 microdeletions in adults with familial tetralogy of Fallot

      GENETICS IN MEDICINE
    2. Boycott, KM; Maybaum, TA; Naylor, MJ; Weleber, RG; Robitaille, J; Miyake, Y; Bergen, AAB; Pierpont, ME; Pearce, WG; Bech-Hansen, NT
      A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

      HUMAN GENETICS
    3. Marin-Garcia, J; Goldenthal, MJ; Ananthakrishnan, R; Pierpont, ME
      The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations

      JOURNAL OF CARDIAC FAILURE
    4. Marin-Garcia, J; Ananthakrishnan, R; Goldenthal, MJ; Pierpont, ME
      Biochemical and molecular basis for mitochondrial cardiomyopathy in neonates and children

      JOURNAL OF INHERITED METABOLIC DISEASE
    5. Helton, E; Darragh, R; Francis, P; Fricker, FJ; Jue, K; Koch, G; Mair, D; Pierpont, ME; Prochazka, JV; Linn, LS; Winter, SC
      Metabolic aspects of myocardial disease and a role for L-carnitine in the treatment of childhood cardiomyopathy

      PEDIATRICS
    6. Sanderson, S; Gross, K; Lulich, J; Osborne, C; Ogburn, P; Pierpont, ME; Koehler, L; Swanson, L; Bird, K; Ulrich, L
      Reliability of taurine concentrations measured in single urine samples obtained from dogs eight hours after eating

      AMERICAN JOURNAL OF VETERINARY RESEARCH
    7. GIBBONS RJ; BACHOO S; PICKETTS DJ; AFTIMOS S; ASENBAUER B; BERGOFFEN J; BERRY SA; DAHL N; FRYER A; KEPPLER K; KUROSAWA K; LEVIN ML; MASUNO M; NERI G; PIERPONT ME; SLANEY SF; HIGGS DR
      MUTATIONS IN TRANSCRIPTIONAL REGULATOR ATRX ESTABLISH THE FUNCTIONAL-SIGNIFICANCE OF A PHD-LIKE DOMAIN

      Nature genetics
    8. SHEFFIELD VC; PIERPONT ME; NISHIMURA D; BEEK JS; BURNS TL; BERG MA; STONE EM; PATIL SR; LAUER RM
      IDENTIFICATION OF A COMPLEX CONGENITAL HEART DEFECT SUSCEPTIBILITY LOCUS BY USING DNA POOLING AND SHARED SEGMENT ANALYSIS

      Human molecular genetics
    9. MARINGARCIA J; IIU YP; ANANTHAKRISHNAN R; PIERPONT ME; PIERPONT GL; GOLDENTHAL MJ
      A POINT MUTATION IN THE CYTB GENE OF CARDIAC MTDNA ASSOCIATED WITH COMPLEX-III DEFICIENCY IN ISCHEMIC CARDIOMYOPATHY

      Biochemistry and molecular biology international
    10. MARINGARCIA J; ANANTHAKRISHNAN R; PIERPONT ME; GOLDENTHAL MJ
      MITOCHONDRIAL DYSFUNCTION IN SPONTANEOUS INBRED TURKEY CARDIOMYOPATHY

      Biochemistry and molecular biology international
    11. PIERPONT GL; EINZIG S; PIERPONT ME; NOREN GR
      THE ETIOLOGY OF LEFT-VENTRICULAR DYSFUNCTION CAN EFFECT THE CATECHOLAMINE RESPONSE TO HEART-FAILURE - CATECHOLAMINES IN HEART-FAILURE

      ACP. Applied cardiopulmonary pathophysiology
    12. SANDERSON S; GROSS KL; OSBORNE CA; LULICH J; OGBUM P; PIERPONT ME; BIRD K; KOEHLER L; SWANSON L; ULRICH L
      DOGS FED A HIGH-FAT DIET HAVE REDUCED PLASMA-CONCENTRATIONS

      The FASEB journal
    13. SANDERSON S; OSBORNE C; LULICH J; PIERPONT ME; GROSS K; OGBURN P; KOEHLER L; CARVALHO M
      RELIABILITY OF CARNITINE CONCENTRATIONS MEASURED IN SINGLE POSTPRANDIAL URINE SAMPLES FROM DOGS

      American journal of veterinary research
    14. SCHIMMENTI LA; PIERPONT ME; CARPENTER BLM; KASHTAN CE; JOHNSON MR; DOBYNS WB
      AUTOSOMAL-DOMINANT OPTIC-NERVE COLOBOMAS, VESICOURETERAL REFLUX, AND RENAL ANOMALIES

      American journal of medical genetics
    15. ALONSO S; PIERPONT ME; RADTKE W; MARTINEZ J; CHEN SC; GRANT JW; DAHNERT I; TAVIAUX S; ROMEY MC; DEMAILLE J; BOUVAGNET P
      HETEROTAXIA SYNDROME AND AUTOSOMAL-DOMINANT INHERITANCE

      American journal of medical genetics
    16. CONRAD B; DEWALD G; CHRISTENSEN E; LOPEZ M; HIGGINS J; PIERPONT ME
      CLINICAL PHENOTYPE ASSOCIATED WITH TERMINAL 2Q37 DELETION

      Clinical genetics
    17. SLETTEN LJ; PIERPONT ME
      CLINICAL SEVERITY OF CONGENITAL HEART-DISEASE IN HOLT-ORAM SYNDROME

      American journal of human genetics
    18. HIGGINS RR; MOREY MA; FERTITTA A; RYHN S; MCCORD J; PIERPONT ME; BURSTEIN L; BREKKEN D; AHMAD J
      USING FISH TO FURTHER DESCRIBE 2 PATIENTS WITH THE CYTOGENETIC ABERRATIONS DUP(17)(P11.2-]P12) AND DEL(4)(P16.3)

      American journal of human genetics
    19. COUSINEAU AJ; LAUER RM; PIERPONT ME; BURNS TL; ARDINGER RH; PATIL SR; SHEFFIELD VC
      LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT ATRIOVENTRICULAR-CANAL DEFECTS- EXCLUSION OF CHROMOSOME-21

      Human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/05/20 alle ore 12:43:31