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 ' Buchholz, T' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 23 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Pihusch, R; Buchholz, T; Lohse, P; Rubsamen, H; Rogenhofer, N; Hasbargen, U; Hiller, E; Thaler, CJ
      Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester

      AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
    2. Runte, M; Farber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Burger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K
      Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Buchholz, T; Molitor, G; Lukong, KE; Praun, M; Genzel-Boroviczeny, O; Freund, M; Pshezhetsky, AV; Schulze, A
      Clinical presentation of congenital sialidosis in a patient with a neuraminidase gene frameshift mutation

      EUROPEAN JOURNAL OF PEDIATRICS
    4. Clement-Sengewald, A; Buchholz, T; Schutze, K
      Laser microdissection as a new approach to prefertilization genetic diagnosis

      PATHOBIOLOGY
    5. Lukong, KE; Elsliger, MA; Chang, Y; Richard, C; Thomas, G; Carey, W; Tylki-Szymanska, A; Czartoryska, B; Buchholz, T; Criado, GR; Palmeri, S; Pshezhetsky, AV
      Characterization of the sialidase molecular defects in sialidosis patientssuggests the structural organization of the lysosomal multienzyme complex

      HUMAN MOLECULAR GENETICS
    6. Newman, LA; Hunt, KK; Buchholz, T; Kuerer, HM; Vlastos, G; Mirza, N; Ames, FC; Ross, MI; Singletary, SE
      Presentation, management and outcome of axillary recurrence from breast cancer

      AMERICAN JOURNAL OF SURGERY
    7. Buchholz, T; Wild, U; Muhler, M; Resofszki, G; Paal, Z
      Hydroisomerization of n-hexane over Pt/sulfated zirconia: activity, reversible deactivation, and surface analysis

      APPLIED CATALYSIS A-GENERAL
    8. Paal, Z; Wild, U; Muhler, M; Manoli, JM; Potvin, C; Buchholz, T; Sprenger, S; Resofszki, G
      The possible reasons of irreversible deactivation of Pt/sulfated zirconia catalysts: structural and surface analysis

      APPLIED CATALYSIS A-GENERAL
    9. Buchholz, T; Klein, A; Kutrib, M
      On time reduction and simulation in cellular spaces

      INTERNATIONAL JOURNAL OF COMPUTER MATHEMATICS
    10. ELLAWAY C; BUCHHOLZ T; SMITH A; LEONARD H; CHRISTODOULOU J
      RETT-SYNDROME - SIGNIFICANT CLINICAL OVERLAP WITH ANGELMAN-SYNDROME BUT NOT WITH METHYLATION STATUS

      Journal of child neurology
    11. Buchholz, T; Jackson, J; Robson, L; Smith, A
      Evaluation of methylation analysis for diagnostic testing in 258 referralssuspected of Prader-Willi or Angelman syndromes

      HUMAN GENETICS
    12. MANOLI JM; POTVIN C; MUHLER M; WILD U; RESOFSZKI G; BUCHHOLZ T; PAAL Z
      EVOLUTION OF THE CATALYTIC ACTIVITY IN PT SULFATED ZIRCONIA CATALYSTS- STRUCTURE, COMPOSITION, AND CATALYTIC PROPERTIES OF THE CATALYST PRECURSOR AND THE CALCINED CATALYST

      Journal of catalysis (Print)
    13. BUITING K; DITTRICH B; GROSS S; LICH C; FARBER C; BUCHHOLZ T; SMITH E; REIS A; BURGER J; NOTHEN MM; BARTHWITTE U; JANSSEN B; ABELIOVICH D; LERER I; VANDENOUWELAND AMW; HALLEY DJJ; SCHRANDERSTUMPEL C; SMEETS H; MEINECKE P; MALCOLM S; GARDNER A; LALANDE M; NICHOLLS RD; FRIEND K; SCHULZE A; MATTHIJS G; KOKKONEN H; HILBERT P; VANMALDERGEM L; GLOVER G; CARBONELL P; WILLEMS P; GILLESSENKAESBACH G; HORSTHEMKE B
      SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS

      American journal of human genetics
    14. BUCHHOLZ T; KUTRIB M
      ON TIME COMPUTABILITY OF FUNCTIONS IN ONE-WAY CELLULAR-AUTOMATA

      Acta informatica
    15. BUCHHOLZ T; KUTRIB M
      SOME RELATIONS BETWEEN MASSIVELY-PARALLEL ARRAYS

      Parallel computing
    16. BUCHHOLZ T; JACKSON J; SMITH A
      METHYLATION ANALYSIS AT 3 DIFFERENT LOCI WITHIN THE IMPRINTED REGION OF CHROMOSOME 15Q11-13

      American journal of medical genetics
    17. SANDANAM T; BEANGE H; ROBSON L; WOOLNOUGH H; BUCHHOLZ T; SMITH A
      MANIFESTATIONS IN INSTITUTIONALIZED ADULTS WITH ANGELMAN SYNDROME DUETO DELETION

      American journal of medical genetics
    18. BUCHHOLZ T; SCHULZE BW
      ANISOTROPIC EDGE PSEUDODIFFERENTIAL-OPERATORS WITH DISCRETE ASYMPTOTICS

      Mathematische Nachrichten
    19. SMITH A; BUCHHOLZ T; ROBSON L
      DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - RESPONSE

      American journal of human genetics
    20. SCHUFFENHAUER S; BUCHHOLZ T; STENGELRUTKOWSKI S; BUITING K; SCHMIDT H; MEITINGER T
      A FAMILIAL DELETION IN THE PRADER-WILLI-SYNDROME REGION INCLUDING THEIMPRINTING CONTROL REGION

      Human mutation
    21. HUNT R; BUCHHOLZ T; ELDER L; HADEN B
      VERIFICATION OF THE PERFORMANCE OF A NEW LIQUID STABILIZED TUMOR-MARKER CONTROL

      Clinical chemistry
    22. SCHUFFENHAUER S; BARTSCH O; STUMM M; BUCHHOLZ T; PETROPOULOU T; KRAFT S; BELOHRADSKY B; HINKEL GK; MEITINGER T; WEGNER RD
      DNA, FISH AND COMPLEMENTATION STUDIES IN ICF SYNDROME - DNA HYPOMETHYLATION OF REPETITIVE AND SINGLE-COPY LOCI AND EVIDENCE FOR A TRANS-ACTING FACTOR

      Human genetics
    23. ALKEMPER J; BUCHHOLZ T; MURAKAMI K; RATKE L
      SOLIDIFICATION OF ALUMINUM-ALLOYS IN AEROGEL MOLDS

      Journal of non-crystalline solids


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 00:28:18