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La ricerca find articoli where soggetti phrase all words 'GENETIC COUNSELING' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 351 riferimenti
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    1. Wheeler, PG; Smith, R; Dorkin, H; Parad, RB; Comeau, AM; Bianchi, DW
      Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical center

      GENETICS IN MEDICINE
    2. Kauff, ND; Scheuer, L; Robson, ME; Glogowski, E; Kelly, B; Barakat, R; Heerdt, A; Borgen, PI; Davis, JG; Offit, K
      Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutations

      GENETICS IN MEDICINE
    3. Velicer, CM; Taplin, S
      Genetic testing for breast cancer: Where are health care providers in the decision process?

      GENETICS IN MEDICINE
    4. Culver, JO; Hull, JL; Dunne, DFB; Burke, W
      Oncologists' opinions on genetic testing for breast and ovarian cancer

      GENETICS IN MEDICINE
    5. Lesca, G; Ollagnon-Roman, E; Lachanat, J; Dusser, A; Edery, P; Jeanpierre, M; Plauchu, H
      Problems in the diagnosis and implications in genetic counseling for a family affected by two distinct neuromuscular disorders.

      ARCHIVES DE PEDIATRIE
    6. Olopade, OI; Pichert, G
      Cancer genetics in oncology practice

      ANNALS OF ONCOLOGY
    7. Schoen, EJ; Limata, C; Black, SB
      Unsuccessful voluntary prenatal testing for human immunodeficiency virus infection

      PEDIATRIC INFECTIOUS DISEASE JOURNAL
    8. Meiser, B; Butow, PN; Barratt, AL; Schnieden, V; Gattas, M; Kirk, J; Gaff, C; Suthers, G; Tucker, K
      Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancer

      PATIENT EDUCATION AND COUNSELING
    9. Tercyak, KP; Johnson, SB; Roberts, SF; Cruz, AC
      Psychological response to prenatal genetic counseling and amniocentesis

      PATIENT EDUCATION AND COUNSELING
    10. Yaegashi, N; Uehara, S; Maeda, T; Fujimori, K; Okamura, K; Yajima, A
      Observed versus expected rates of unbalanced fetal karyotype at second trimester amniocentesis when one parent carries a balanced translocation

      GYNECOLOGIC AND OBSTETRIC INVESTIGATION
    11. Tercyak, KP; Lerman, C; Peshkin, BN; Hughes, C; Main, D; Isaacs, C; Schwartz, MD
      Effects of coping style and BRCA1 and BRCA2 test results on anxiety among women participating in genetic counseling and testing for breast and ovarian cancer risk

      HEALTH PSYCHOLOGY
    12. Sagi, M; Meiner, V; Reshef, N; Dagan, J; Zlotogora, J
      Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for highrates of pregnancy termination

      PRENATAL DIAGNOSIS
    13. Kallinen, J; Heinonen, S; Palotie, A; Mannermaa, A; Ryynanen, M
      Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in Finland

      PRENATAL DIAGNOSIS
    14. Peters, J; Loud, J; Dimond, E; Jenkins, J
      Cancer genetics fundamentals

      CANCER NURSING
    15. Fanos, JH; Davis, J; Puck, JM
      Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Fanos, JH; Puck, JM
      Family pictures: Growing up with a brother with X-linked severe combined immunodeficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Biesecker, BB; Peters, KF
      Process studies in genetic counseling: Peering into the black box

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Benkendorf, JL; Prince, MB; Rose, MA; De Fina, A; Hamilton, HE
      Does indirect speech promote nondirective genetic counseling? Results of asociolinguistic investigation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Wang, VO
      Multicultural genetic counseling: Then, now, and in the 21st century

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Guttmacher, AE; Jenkins, J; Uhlmann, WR
      Genomic medicine: Who will practice it? A call to open arms

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Greendale, K; Pyeritz, RE
      Empowering primary care health professionals in medical genetics: How soon? How fast? How far?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    22. Burke, W; Pinsky, LE; Press, NA
      Categorizing genetic tests to identify their ethical, legal, and social implications

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Thorburn, DR; Dahl, HHM
      Mitochondrial disorders: Genetics, counseling, prenatal diagnosis and reproductive options

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Maat-Kievit, A; Helderman-van den Enden, P; Losekoot, M; de Knijff, P; Belfroid, R; Vegter-van der Vlis, M; Roos, R; Breuning, M
      Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Rosenthal, ET; Biesecker, LG; Biesecker, BB
      Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Green, MJ; Biesecker, BB; McInerney, AM; Mauger, D; Fost, N
      An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Green, MJ; McInerney, AM; Biesecker, BB; Fost, N
      Education about genetic testing for breast cancer susceptibility: Patient preferences for a computer program or genetic counselor

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Ciske, DJ; Haavisto, A; Laxova, A; Rock, LZM; Farrell, PM
      Genetic counseling and neonatal screening for cystic fibrosis: An assessment of the communication process

      PEDIATRICS
    29. Brunger, JW; Matthews, AL; Smith, RHJ; Robin, NH
      Genetic testing and genetic counseling for deafness: The future is here

      LARYNGOSCOPE
    30. Paterson, CR; Monk, EA; McAllion, SJ
      How common is hearing impairment in osteogenesis imperfecta?

      JOURNAL OF LARYNGOLOGY AND OTOLOGY
    31. Fujisawa, M; Shirakawa, T; Kanzaki, M; Okada, H; Arakawa, S; Kamidono, S
      Y-chromosome microdeletion and phenotype in cytogenetically normal men with idiopathic azoospermia

      FERTILITY AND STERILITY
    32. Wong, N; Lasko, D; Rabelo, R; Pinsky, L; Gordon, PH; Foulkes, W
      Genetic counseling and interpretation of genetic tests in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer

      DISEASES OF THE COLON & RECTUM
    33. Biesecker, BB
      Goals of genetic counseling

      CLINICAL GENETICS
    34. Peters, KF; Kong, F; Horne, R; Francomano, CA; Biesecker, BB
      Living with Marfan syndrome I. Perceptions of the condition

      CLINICAL GENETICS
    35. Dagan, E; Gershoni-Baruch, R
      Hereditary breast/ovarian cancer - pitfalls in genetic counseling

      CLINICAL GENETICS
    36. Weil, J
      Multicultural education and genetic counseling

      CLINICAL GENETICS
    37. Schwartz, MD; Benkendorf, J; Lerman, C; Isaacs, C; Ryan-Robertson, A; Johnson, L
      Impact of educational print materials on knowledge, attitudes, and interest in BRCA1/BRCA2 - Testing among Ashkenazi Jewish women

      CANCER
    38. Kinney, AY; DeVellis, BM; Skrzynia, C; Millikan, R
      Genetic testing for colorectal carcinoma susceptibility - Focus group responses of individuals with colorectal carcinoma and first-degree relatives

      CANCER CYTOPATHOLOGY
    39. Kinney, AY; DeVellis, BM; Skrzynia, C; Millikan, R
      Genetic testing for colorectal carcinoma susceptibility - Focus group responses of individuals with colorectal carcinoma and first-degree relatives

      CANCER
    40. Morris, KT; Johnson, N; Krasikov, N; Allen, M; Dorsey, P
      Genetic counseling impacts decision for prophylactic surgery for patients perceived to be at high risk for breast cancer

      AMERICAN JOURNAL OF SURGERY
    41. Sperling, L; Tabor, A
      Twin pregnancy: the role of ultrasound in management

      ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
    42. Karp, SE
      Clinical management of BRCA1-and BRCA2-associated breast cancer

      SEMINARS IN SURGICAL ONCOLOGY
    43. Lynch, HT; Lynch, JF
      Hereditary nonpolyposis colorectal cancer

      SEMINARS IN SURGICAL ONCOLOGY
    44. Lal, G; Gallinger, S
      Familial adenomatous polyposis

      SEMINARS IN SURGICAL ONCOLOGY
    45. Kash, KM; Ortega-Verdejo, K; Dabney, MK; Holland, JC; Miller, DG; Osborne, MP
      Psychosocial aspects of cancer genetics: Women at high risk for breast andovarian cancer

      SEMINARS IN SURGICAL ONCOLOGY
    46. Anderlik, MR; Lisko, EA
      Medicolegal and ethical issues in genetic cancer syndromes

      SEMINARS IN SURGICAL ONCOLOGY
    47. Stopfer, JE
      Genetic counseling and clinical cancer genetics services

      SEMINARS IN SURGICAL ONCOLOGY
    48. Barcus, ME; Ferriera-Gonzalez, A; Buller, AM; Wilkinson, DS; Garrett, CT
      Genetic changes in solid tumors

      SEMINARS IN SURGICAL ONCOLOGY
    49. Keller, M
      Psychosocial issues in cancer genetics: State of the art

      ZEITSCHRIFT FUR PSYCHOSOMATISCHE MEDIZIN UND PSYCHOTHERAPIE
    50. Henderson, LB; Adams, JS; Goldstein, DR; Braunstein, GD; Rotter, JI; Scheuner, MT
      A familial risk profile for osteoporosis

      GENETICS IN MEDICINE
    51. Filocamo, M; Bonuccelli, G; Mazzotti, R; Corsolini, F; Stroppiano, M; Regis, S; Gatti, R
      Somatic mosaicism in a patient with Gaucher disease type 2: Implication for genetic counseling and therapeutic decision-making

      BLOOD CELLS MOLECULES AND DISEASES
    52. Filocamo, M; Bonuccelli, G; Mazzotti, R; Giona, F; Gatti, R
      Identification of a novel recombinant allele in three unrelated Italian Gaucher patients: Implications for prognosis and genetic counseling

      BLOOD CELLS MOLECULES AND DISEASES
    53. Kinney, AY; Choi, YA; DeVellis, B; Millikan, R; Kobetz, E; Sandler, RS
      Attitudes toward genetic testing in patients with colorectal cancer

      CANCER PRACTICE
    54. Diefenbach, MA; Schnoll, RA; Miller, SM; Brower, L
      Genetic testing for prostate cancer - Willingness and predictors of interest

      CANCER PRACTICE
    55. Girodon-Boulandet, E; Cazeneuve, C; Goossens, M
      Screening practices for mutations in the CFTR gene ABCC7

      HUMAN MUTATION
    56. Hofferbert, S; Worringen, U; Backe, J; Ruckert, EM; White, K; Faller, H; Grimm, T; Caffier, H; Chang-Claude, J; Weber, BHF
      Simultaneous interdisciplinary counseling in German breast/ovarian cancer families: First experiences with patient perceptions, surveillance behaviorand acceptance of genetic testing

      GENETIC COUNSELING
    57. Julia, S; Beth, E
      Genetic counseling and cystic fibrosis

      REVUE DES MALADIES RESPIRATOIRES
    58. Hai, N; Kosugi, S
      Gene diagnosis and clinical management of multiple endocrine neoplasia type 1 (MEN1)

      BIOMEDICINE & PHARMACOTHERAPY
    59. Tagariello, G; Belvini, D; Salviato, R; Are, A; De Biasi, E; Goodeve, A; Davoli, P
      Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosis

      HAEMATOLOGICA
    60. Fineman, RM; Walton, MT
      Should genetic health care providers attempt to influence reproductive outcome using directive counseling techniques? A public health prospective

      WOMEN & HEALTH
    61. Williams, JK; Schutte, DL; Evers, C; Holkup, PA
      Redefinition: Coping with normal results from predictive gene testing for neurodegenerative disorders

      RESEARCH IN NURSING & HEALTH
    62. Williams, JK; Schutte, DL; Holkup, PA; Evers, C; Muilenburg, A
      Psychosocial impact of predictive testing for Huntington disease on support persons

      AMERICAN JOURNAL OF MEDICAL GENETICS
    63. Braga, MCC; Otto, PA; Frota-Pessoa, O
      Calculation of recurrence risks for heterogeneous genetic disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    64. Bernhardt, BA; Biesecker, BB; Mastromarino, CL
      Goals, benefits, and outcomes of genetic counseling: Client and genetic counselor assessment

      AMERICAN JOURNAL OF MEDICAL GENETICS
    65. Biesecker, BB; Ishibe, N; Hadley, DW; Giambarresi, TR; Kase, RG; Lerman, C; Struewing, JP
      Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    66. McConkie-Rosell, A; Spiridigliozzi, GA; Sullivan, JA; Dawson, DV; Lachiewicz, AM
      Carrier testing in fragile X syndrome: Effect on self-concept

      AMERICAN JOURNAL OF MEDICAL GENETICS
    67. Cooper, HA; Crowe, J; Butler, MG
      SPONASTRIME dysplasia: Report of an 11-year-old boy and review of the literature

      AMERICAN JOURNAL OF MEDICAL GENETICS
    68. Finckh, U; Schroder, J; Ressler, B; Veske, A; Gal, A
      Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    69. Johnson, KA; Rosenblum-Vos, L; Petersen, GM; Brensinger, JD; Giardiello, FM; Griffin, CA
      Response to genetic counseling and testing for the APC I1307K mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    70. Burke, W; Culver, JO; Bowen, D; Lowry, D; Durfy, S; McTiernan, A; Andersen, MR
      Genetic counseling for women with an intermediate family history of breastcancer

      AMERICAN JOURNAL OF MEDICAL GENETICS
    71. Menasha, JD; Schechter, C; Willner, J
      Genetic testing: A physician's perspective

      MOUNT SINAI JOURNAL OF MEDICINE
    72. Balmana, J; Brunet, J; Capella, G; Gonzalez, D; Palicio, M; Sancho, FJ; Pericay, C; Lopez, JJL; Marcuello, E
      Identification of two families with hereditary nonpolyposis colorectal cancer and Amsterdam criteria. Relevance of family history and follow-up

      MEDICINA CLINICA
    73. Daudin, M; Bieth, E; Bujan, L; Massat, G; Pontonnier, F; Mieusset, R
      Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling

      FERTILITY AND STERILITY
    74. Sarroca, C; Alfano, N; Bendin, GT; Della Valle, A; Dominguez, A; Quadrelli, R; Vaglio, A; Mechoso, B; Tinley, ST; Harty, AE; Lynch, JF; Franklin, BA; Kristo, P; Smyrk, TC; Peltomaki, P; Lynch, HT
      Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay

      DISEASES OF THE COLON & RECTUM
    75. Bennett, RL
      Pedigree parables

      CLINICAL GENETICS
    76. Gershon, ES
      Bipolar illness and schizophrenia as oligogenic diseases: Implications forthe future

      BIOLOGICAL PSYCHIATRY
    77. Li, CC
      Progressing from eugenics to human genetics - Celebrating the 70th birthday of Professor Newton E. Morton

      HUMAN HEREDITY
    78. Wakui, K; Tanemura, M; Suzumori, K; Hidaka, E; Ishikawa, M; Kubota, T; Fukushima, Y
      Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies

      JOURNAL OF HUMAN GENETICS
    79. Pimentel, MMG
      Fragile X syndrome

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    80. Callanan, NP; Cheuvront, BJ; Sorenson, JR
      CF Carrier testing in a high risk population: Anxiety, risk perceptions, and reproductive plans of carrier by 'non-carrier' couples

      GENETICS IN MEDICINE
    81. Bennett, RL; Hudgins, L; Smith, CO; Motulsky, AG
      Inconsistencies in genetic counseling and screening for consanguineous couples and their offspring: The need for practice guidelines

      GENETICS IN MEDICINE
    82. Barton, JC; Rothenberg, BE; Bertoli, LF; Acton, RT
      Diagnosis of hemochromatosis in family members of probands: A comparison of phenotyping and HFE genotyping

      GENETICS IN MEDICINE
    83. Ko, TM; Hwu, WL; Lin, YW; Tseng, LH; Hwa, HL; Wang, TR; Chuang, SM
      Molecular genetic study of Pompe disease in Chinese patients in Taiwan

      HUMAN MUTATION
    84. Suzuki, A; Takenoshita, Y; Honda, Y; Matsuura, C
      Dentocraniofacial morphology in parents of children with cleft lip and/or palate

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    85. Sigler, A; Ontiveros, DS
      Nasal deformity and microform cleft lip in parents of patients with cleft lip

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    86. Hashimoto, I; Kon, A; Tamai, K; Uitto, J
      Diagnostic dilemma of "sporadic" cases of dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?

      EXPERIMENTAL DERMATOLOGY
    87. Demsey, SA
      Carrier screening for cystic fibrosis: A perinatal perspective

      JOURNAL OF PERINATAL & NEONATAL NURSING
    88. Lovestone, S
      Early diagnosis and the clinical genetics of Alzheimer's disease

      JOURNAL OF NEUROLOGY
    89. Bird, TD
      Risks and benefits of DNA testing for neurogenetic disorders

      SEMINARS IN NEUROLOGY
    90. Jospe, ES; Peppercorn, MA
      Inflammatory bowel disease and pregnancy: A review

      DIGESTIVE DISEASES
    91. Loescher, LJ
      The family history component of cancer genetic risk counseling

      CANCER NURSING
    92. Spahis, JK; Wilson, GN
      Down syndrome: Perinatal complications and counseling experiences in 216 patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    93. Fanos, JH; Mackintosh, MA
      Never again joy without sorrow: The effect on parents of a child with ataxia-telangiectasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    94. Fanos, JH
      "My crooked vision": The well sib views ataxia-telangiectasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Eggers, S; Pavanello, RCM; Passos-Bueno, MR; Zatz, M
      Genetic counseling for childless women at risk for Duchenne muscular dystrophy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Fanos, JH; Gatti, RA
      A mark on the arm: Myths of carrier status in sibs of individuals with ataxia-telangiectasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    97. Pollin, TI; Dobyns, WB; Crowe, CA; Ledbetter, DH; Bailey-Wilson, JE; Smith, ACM
      Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Cho, MK; Sankar, P; Wolpe, PR; Godmilow, L
      Commercialization of BRCA1/2 testing: Practitioner awareness and use of a new genetic test

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. McConkie-Rosell, A; Spiridigliozzi, GA; Rounds, K; Dawson, DV; Sullivan, JA; Burgess, D; Lachiewicz, AM
      Parental attitudes regarding carrier testing in children at risk for fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    100. Guze, CD; Hyman, PE; Payne, VJ
      Family studies of infantile visceral myopathy: A congenital myopathic pseudo-obstruction syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS


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Documento generato il 28/10/20 alle ore 02:13:45