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 ' DALPRA L' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 50 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Ferrarese, C; Tremolizzo, L; Rigoldi, M; Sala, G; Begni, B; Brighina, L; Ricci, G; Albizzati, MG; Piolti, R; Crosti, F; Dalpra, L; Frattola, L
      Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease

      NEUROLOGICAL SCIENCES
    2. Duga, S; Solda, G; Asselta, R; Bonati, MT; Dalpra, L; Malcovati, M; Tenchini, ML
      Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms

      JOURNAL OF HUMAN GENETICS
    3. Borgatti, R; Piccinelli, P; Passoni, D; Dalpra, L; Miozzo, M; Micheli, R; Gagliardi, C; Balottin, U
      Relationship between clinical and genetic features in "inverted duplicatedchromosome 15" patients

      PEDIATRIC NEUROLOGY
    4. Villa, N; Riva, P; Colombo, D; Sala, E; Mariani, S; Zorloni, C; Crosti, F; Dalpra, L
      Identification of a small supernumerary marker chromosome, r(2)(p10q11.2),and the problem of determining prognosis

      PRENATAL DIAGNOSIS
    5. Pallotta, R; Dalpra, L; Miozzo, M; Ehresmann, T; Fusilli, P
      A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Bonati, MT; Asselta, R; Duga, S; Ferini-Strambi, L; Oldani, A; Zucconi, M; Malcovati, M; Dalpra, L; Tenchini, ML
      Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE

      NEUROREPORT
    7. Bonati, MT; Duga, S; Asselta, R; Ferini-Strambi, L; Oldani, A; Zucconi, M; Malcovati, M; Dalpra, L; Tenchini, ML
      A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker

      MOLECULAR AND CELLULAR PROBES
    8. Marozzi, A; Manfredini, E; Tibiletti, MG; Furlan, D; Villa, N; Vegetti, W; Crosignani, PG; Ginelli, E; Meneveri, R; Dalpra, L
      Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure

      HUMAN GENETICS
    9. Vegetti, W; Marozzi, A; Manfredini, E; Testa, G; Alagna, F; Nicolosi, A; Caliari, I; Taborelli, M; Tibiletti, MG; Dalpra, L; Crosignani, PG
      Premature ovarian failure

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    10. Marozzi, A; Vegetti, W; Manfredini, E; Tibiletti, MG; Testa, G; Crosignani, PG; Ginelli, E; Meneveri, R; Dalpra, L
      Association between idiopathic premature ovarian failure and fragile X premutation

      HUMAN REPRODUCTION
    11. Riva, P; Dalpra, L; Gualandri, V; Volonte, M; Miozzo, M; Malgara, R; Conti, AF; Larizza, L
      19p deletion in recurring leiomyosarcoma lesions from the same patient

      CANCER GENETICS AND CYTOGENETICS
    12. Villa, N; Sala, E; Colombo, D; Dell'Orto, M; Grioni, D; Dalpra, L
      Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocation

      JOURNAL OF MEDICAL GENETICS
    13. Miozzo, M; Dalpra, L; Riva, P; Volonte, M; Macciardi, F; Pericotti, S; Tibiletti, MG; Cerati, M; Rohde, K; Larizza, L; Conti, AMF
      A tumor suppressor locus in familial and sporadic chordoma maps to 1p36

      INTERNATIONAL JOURNAL OF CANCER
    14. Marozzi, A; Dalpra, L; Ginelli, E; Tibiletti, MG; Crosignani, PG
      FRAXA premutations are not a cause of familial premature ovarian failure

      HUMAN REPRODUCTION
    15. Tibiletti, MG; Testa, G; Vegetti, W; Alagna, F; Taborelli, M; Dalpra, L; Bolis, PF; Crosignani, PG
      The idiopathic forms of premature menopause and early menopause show the same genetic pattern

      HUMAN REPRODUCTION
    16. Tenchini, ML; Duga, S; Bonati, MT; Asselta, R; Oldani, A; Zucconi, M; Malcovati, M; Dalpra, L; Ferini-Strambi, L
      SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the ItalianADNFLE population

      SLEEP
    17. Dalpra, L; Malgara, R; Miozzo, M; Riva, P; Volonte, M; Larizza, L; Conti, AMF
      First cytogenetic study of a recurrent familial chordoma of the clivus

      INTERNATIONAL JOURNAL OF CANCER
    18. MAROZZI A; DALPRA L; MIOZZO M; TABORELLI M; TIBILETTI MG; VEGETTI W; TESTA G; CROSIGNANI DG; GINELLI E
      GENETIC-CHARACTERIZATION OF A FAMILIAL POF SAMPLE

      European journal of human genetics
    19. TABORELLI M; DELCURTO A; FURLAN D; TESTA G; VEGETTI W; DALPRA L; TIBILETTI MG
      INHERITANCE IN IDIOPATHIC PREMATURE OVARIAN FAILURE - ANALYSIS OF 71 CASES

      European journal of human genetics
    20. VILLA N; SALA E; COLOMBO D; GRIONI D; DALPRA L
      REPRODUCTIVE OUTCOME IN A FAMILY WITH A SATELLITED CHROMOSOME-1

      European journal of human genetics
    21. MIOZZO M; NOCERA G; VILLA N; SALA E; ILARDI P; CONTI AMF; DALPRA L
      UPD TESTING IN PRENATALLY NOT-CONFIRMED CHROMOSOME MOSAICISM

      European journal of human genetics
    22. RIVA P; MALGARA R; DALPRA L; VOLONTE M; GUALANDRI V; CONTI AMF; LARIZZA L
      19P13.12-PTER DELETION IN MULTIPLE LEIOMYOSARCOMAS FROM THE SAME PATIENT

      Cytogenetics and cell genetics
    23. VEGETTI W; TIBILETTI MG; TESTA G; YANKOWSKI LD; ALAGNA F; CASTOLDI E; TABORELLI M; MOTTA T; BOLIS PF; DALPRA L; CROSIGNANI PG
      INHERITANCE IN IDIOPATHIC PREMATURE OVARIAN FAILURE - ANALYSIS OF 71 CASES

      Human reproduction (Oxford. Print)
    24. TESTA G; VEGETTI W; FURLAN D; PRATO D; TIBILETTI MG; DALPRA L; CASTOLDI E; ALAGNA F; BOLIS PF; CROSIGNANI PG
      INHERITANCE IN IDIOPATHIC PREMATURE OVARIAN FAILURE - ANALYSIS OF 71 CASES

      Human reproduction (Oxford. Print)
    25. ALAGNA F; TESTA G; VEGETTI W; TABORELLI M; DELCURTO A; LALIA M; YANKOWSKI LD; TIBILETTI MG; DALPRA L; BOLIS PF; CROSIGNANI PG
      ARE PREMATURE OVARIAN FAILURE (POF) AND EARLY MENOPAUSE THE SAME ENTITY

      Human reproduction (Oxford. Print)
    26. RUSSO S; SELICORNI A; BEDESCHI MF; NATACCI F; VIZIELLO P; FORTUNA R; PAGANI G; DALPRA L; LARIZZA L
      MOLECULAR CHARACTERIZATION OF FRAXE-POSITIVE SUBJECTS WITH MENTAL IMPAIRMENT IN 2 UNRELATED ITALIAN FAMILIES

      American journal of medical genetics
    27. MIOZZO M; CASTORINA P; RIVA P; DALPRA L; CONTI AMF; VOLPI L; HOE TS; KHOO A; WIEGANT J; ROSENBERG C; LARIZZA L
      CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME

      International journal of cancer
    28. OLDANI A; ZUCCONI M; ASSELTA R; MODUGNO M; BONATI MT; DALPRA L; MALCOVATI M; TENCHINI ML; SMIRNE S; FERINISTRAMBI L
      AUTOSOMAL-DOMINANT NOCTURNAL FRONTAL-LOBE EPILEPSY - A VIDEO-POLYSOMNOGRAPHIC AND GENETIC APPRAISAL OF 40 PATIENTS AND DELINEATION OF THE EPILEPTIC SYNDROME

      Brain
    29. BOLOGNESI C; ABBONDANDOLO A; BARALE R; CASALONE R; DALPRA L; DEFERRARI M; DEGRASSI F; FORNI A; LAMBERTI L; LANDO C; MIGLIORE L; PADOVANI P; PASQUINI R; PUNTONI R; SBRANA I; STELLA M; BONASSI S
      AGE-RELATED INCREASE OF BASE-LINE FREQUENCIES OF SISTER-CHROMATID EXCHANGES, CHROMOSOME-ABERRATIONS, AND MICRONUCLEI IN HUMAN-LYMPHOCYTES

      Cancer epidemiology, biomarkers & prevention
    30. CASTORINA P; MIOZZO M; RIVA P; CONTI AMF; WIEGANT J; ROSENBERG C; DALPRA L; VOLPI L; MAK JW; LARIZZA L
      HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)

      Cytogenetics and cell genetics
    31. COLOMBO D; VILLA N; MIOZZO M; SALA E; CAPPELLINI A; MARIANI S; BORRONI D; DALPRA L
      MULTITECHNICAL APPROACH TO RESOLVE A CASE OF TRISOMY-5 MOSAICISM IN AF CELLS IN A PREGNANCY WITH IUGR

      Cytogenetics and cell genetics
    32. VILLA N; DALPRA L; LARIZZA L
      EXPRESSION OF RARE FRA10Q24 - CHROMOSOME TRUNCATION, AMPLIFICATION OFDISTAL SEGMENT AND TELOMERE RENEWAL

      Cytogenetics and cell genetics
    33. MIOZZO M; MALGARA R; RIVA P; VOLONTE M; LARIZZA L; CONTI AMF; DALPRA L
      CYTOGENETIC CHARACTERIZATION OF A CLIVUS CHORDOMA IN A CANCER FAMILY PATIENT

      Cytogenetics and cell genetics
    34. RIVA P; MALGARA R; DALPRA L; VOLONTE M; GUALANDRI V; CONTI AMF; LARIZZA L
      CYTOGENETIC FINDINGS ON MULTIPLE LEIOMYOSARCOMA THE SAME PATIENT

      Cytogenetics and cell genetics
    35. TESTA G; VEGETTI W; TIBILETTI MG; DALPRA L; DELAURETIS L; LALIA M; ALAGNA F; BOLIS PF; CROSIGNANI PG
      PATTERN OF INHERITANCE IN FAMILIAL PREMATURE OVARIAN FAILURE

      Human reproduction
    36. CASTORINA P; SELICORNI A; BEDESCHI F; DALPRA L; LARIZZA L
      GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME

      American journal of medical genetics
    37. VILLA N; DALPRA L; LARIZZA L
      EXPRESSION OF 3 RARE FRAGILE SITES - CHROMOSOMAL TRUNCATION, AMPLIFICATION OF DISTAL SEGMENT AND TELOMERIC RENEWAL

      Chromosoma
    38. RIVA P; CASTORINA P; MANOUKIAN S; DALPRA L; DONEDA L; MARINI G; DENDUNNEN J; LARIZZA L
      CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME

      Human genetics
    39. PALLOTTA R; DALPRA L; FUSILLI P; ZUFFARDI O
      FURTHER DELINEATION OF 7P TRISOMY - CASE-REPORT AND REVIEW OF LITERATURE

      Annales de genetique
    40. FLORIDIA G; PIANTANIDA M; MINELLI A; DELLAVECCHIA C; BONAGLIA C; ROSSI E; GIMELLI G; CROCI G; FRANCHI F; GILGENKRANTZ S; GRAMMATICO P; DALPRA L; WOOD S; DANESINO C; ZUFFARDI O
      THE SAME MOLECULAR MECHANISM AT THE MATERNAL MEIOSIS-I PRODUCES MONOCENTRIC AND DICENTRIC 8P DUPLICATIONS

      American journal of human genetics
    41. MILANI N; DALPRA L; DELPRETE A; ZANINI R; LARIZZA L
      A NOVEL MUTATION (GLN266-]HIS) IN THE ALPHA1 SUBUNIT OF THE INHIBITORY GLYCINE-RECEPTOR GENE (GLRA1) IN HEREDITARY HYPEREKPLEXIA

      American journal of human genetics
    42. BONASSI S; BOLOGNESI C; ABBONDANDOLO A; BARALE R; BIGATTI P; CAMURRI L; DALPRA L; DEFERRARI M; FORNI A; LANDO C; PADOVANI P; PASQUINI R; STELLA M; PUNTONI R
      INFLUENCE OF SEX ON CYTOGENETIC END-POINTS - EVIDENCE FROM A LARGE HUMAN SAMPLE AND REVIEW OF THE LITERATURE

      Cancer epidemiology, biomarkers & prevention
    43. BONASSI S; ABBONDANDOLO A; CAMURRI L; DALPRA L; DEFERRARI M; DEGRASSI F; FORNI A; LAMBERTI L; LANDO C; PADOVANI P; SBRANA I; VECCHIO D; PUNTONI R
      ARE CHROMOSOME-ABERRATIONS IN CIRCULATING LYMPHOCYTES PREDICTIVE OF FUTURE CANCER ONSET IN HUMANS - PRELIMINARY-RESULTS OF AN ITALIAN COHORT STUDY

      Cancer genetics and cytogenetics
    44. LARIZZA L; RIVA P; CASTORINA P; DALPRA L; DONEDA L; MANOUKIAN S
      CYTOGENETIC AND MOLECULAR STUDIES ON NF1 PATIENTS WITH DYSMORPHISM AND MENTAL-RETARDATION

      American journal of human genetics
    45. MILANI N; DALPRA L; DELPRETE L; ZANINI R; LARIZZA L
      A NEW MISSENSE MUTATION IN EXON-6 OF THE GLYCINE RECEPTOR (GLRA1) GENE IN HEREDITARY HYPEREKPLEXIA

      American journal of human genetics
    46. PITTALIS MC; DALPRA L; TORRICELLI F; RIZZO N; NOCERA G; CARIATI E; SANTARINI L; TIBILETTI MG; AGOSTI S; BOVICELLI L; FORABOSCO A
      THE PREDICTIVE VALUE OF CYTOGENETIC DIAGNOSIS AFTER CVS BASED ON 4860CASES WITH BOTH DIRECT AND CULTURE METHODS

      Prenatal diagnosis
    47. DALPRA L; NOCERA G; TIBILETTI MG; MARTINOLI E; OLDRINI A; AGOSTI S; CROSIGNANI PG
      LATE CHORIONIC VILLUS SAMPLING - CYTOGENETIC ASPECTS

      Prenatal diagnosis
    48. MASTROIACOVO P; TOZZI AE; AGOSTI S; BOCCHINO G; BOVICELLI L; DALPRA L; CARBONE LDL; LITUANIA M; LUTTICHAU A; MANTEGAZZA F; NOCERA G; PACHI A; PASSAMONTI U; PIOMBO G; VASTA AF
      TRANSVERSE LIMB REDUCTION DEFECTS AFTER CHORION VILLUS SAMPLING - A RETROSPECTIVE COHORT STUDY

      Prenatal diagnosis
    49. DONEDA L; DALPRA L; TIBILETTI MG; LARIZZA L
      PRENATAL-DIAGNOSIS OF AN EXTRANUMERARY I(22P) WITH NORMAL PHENOTYPE

      Annales de genetique
    50. DALPRA L; TIBILETTI MG; CRISTIANI C; RAGNI G; CROSIGNANI PG
      MORPHOLOGY AND NUCLEAR CONTENTS IN IVF EMBRYOS

      Annales de genetique


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/01/21 alle ore 03:23:01