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These search results show articles and films where one or more keywords of any type is Cystic fibrosis.
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TitleDateReferenceAuthorsCall #ISSN
Therapeutic endings: reflections of counselling-based research relationships among patients with cystic fibrosis and their caregivers2019 Time and society 28 (1): 358-74
  • Fiona J. Moola
H6 [TIME-]0961-463X
The ecology of care in cystic fibrosis. Identification, decision-making and learning in a community living and working with a rare chronic illness2018 Curare 41 (1-2): 115-33, 168, 175
  • Doris Staab
  • Jörg Niewöhner
  • Stefan Reinsch
H6/KGT [CURARE-]0344-8622in thematic issue 'Healing cooperations. Heterogenous collaborations beyond dyadic interactions'; German and French summaries
When care strikes back - some strategies and tactics for dealing with ambivalence of visibility in chronic illness2016 Irish journal of anthropology 19 (1): 82-90
  • Doris Staab
  • Jörg Niewöhner
  • Stefan Reinsch
H6/KVC [IRISH-]1393-8592in thematic issue on social suffering; with introductory note by K Keohane, 10-11
Association of CFTR gene mutation with bronchial asthma and its severity in Indian children: a case-control study2012 Annals of human biology 39 (2): 113-21
  • Nutan Maurya
  • Pratibha Dixit
  • Sarita Agarwal
  • Shally Awasthi
  • Srinivasan Muthuswamy
H6/HB [ANNALS-]0301-4460
Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa2012 Annals of human biology 39 (1): 76-9
  • A. Bouker
  • M. Boudaya
  • M. Khrouf
  • R. Bel Haj
  • S. Hadj Fredj
H6/HB [ANNALS-]0301-4460
Anthropological features of the CFTR gene: its variability in an African population2011 Annals of human biology 38 (2): 203-9
  • Cinzia Ciccacci
  • Cristina Bombieri
  • Fiorenza Pompei
  • Franca Maria Ciminelli
  • Francesca Belpinati
H6/HB [ANNALS-]0301-4460
Growth and nutritional status in children and adolescents with cystic fibrosis2008 Annals of human biology 35 (2): 145-53
  • Charles Susanne
  • Wioleta Umławska
H6/HB [ANNALS-]0301-4460
Low frequency of the ΔF508 mutation of the CFTR gene in a highly admixed population in Bahia, Brazil2007 Human biology 79 (3): 293-7
  • Angelina Xavier Acosta
  • Antônio Carlos Moreira Lemos
  • Bernardo Galvão-Castro
  • Fabiana Maia Moura Costa
  • Maria Angélica Santana
H6/HB [HUMAN-]0018-7143
Relationship between genotype and anthropological parameters of Slovak patients suffering from cystic fibrosis2006 Česká antropologie 56: 145-8
  • Eva Nešćáková
  • Hana Kayserova
  • Milica Beránková
  • Paula Zajacova
  • Stanislav Katina
  • Zuzana Kapustova
H6/KVL [ANTROPOLOGICKÁ-]0862-5085English summary
Sequence of ΔF 508 CFTR allele identified at present is lacking in medieval specimens from central Poland. Preliminary results2006 Anthropologischer Anzeiger 64 (1): 41-9
  • Anna Wrzesińska
  • Elżbieta Żądzińska
  • Henryk W. Witas
  • Izabela Jatczak
  • Krystyna Jędrychowska-Dańska
H6/HB [ANTHROPOLOGISCHER-]0003-5548German summary
Molecular analysis of 23 exons of the CFTR gene in Brazilian patients leads to the finding of rare cystic fibrosis mutations2005 Human biology 77 (1): 125-35
  • Giselda M. K. Cabello
  • Juan C. Llerena jr
  • Koko Otsuki
  • Maria Emilia Gombarovits
  • Pedro H. Cabello
H6/HB [HUMAN-]0018-7143
Spectrum of CFTR mutations on Réunion Island: impact on neonatal screening2005 Human biology 77 (5): 705-14
  • C. Leroy
  • F. Cartault
  • J. F. Lesure
  • M. Viel
  • T. Bienvenu
H6/HB [HUMAN-]0018-7143
Assessment of the biological condition and nutritional status fo adult patients with cystic fibrosis2005 Przegląd antropologiczny 68: 53-64
  • Anita Szwed
  • Joachim Cieślik
  • Joanna Goździk
  • Karol Karbowy
  • Magdalena Kosińska
H6/KE [PRZEGLAD-]0033-2003Polish summary
What is incidence of cystic fibrosis in Italy ? Data from the National Registry2004 Human biology 76 (3): 455-67
  • Assemblea dei Direttori dei Centri
  • Anna Bossi
  • Giovanna Casazza
  • Rita Padoan
  • Silvano Milani
H6/HB [HUMAN-]0018-7143
Cystic fibrosis mutations in Costa Rica2003 Human biology 75 (2): 179-88
  • Castro A. Oscar
  • Felix L. Sánchez
  • Ines G. Gutiérrez
  • Jessica M. Novak
  • Patricia B. Venegas
0018-7143
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patiens from São Paulo state, Brazil2003 Human biology 75 (3): 393-8
  • Agnes Cristina Fett-Conte
  • Andrea Regina B. Rossit
  • Eny Maria Goloni-Bertollo
  • Joao Batista Salomão jr
  • Salmo Raskin
0018-7143
Nutritional status of Czech patients with cystic fibrosis: is it influenced by diabetes mellitus and insulin therapy ?2003 Anthropologie (Brno) 41 (1-2): 119-22
  • Daniela Zemková
  • Jana Bartošova
  • Milan jr Macek
  • Stanislava Koloušková
  • Vera Vávrová
H6/HB [ANTHROPOLOGIE-]0323-1119
Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients2001 Human biology 73 (2): 191-203
  • Hulya Kayseruku
  • Julian Zielenski
  • Nalan Gokgoz
  • Ozlem Topaloglu
  • Tuncer Onay
0018-7143
The 3120 +1G→A splicing mutation in CFTR is common in Brazilian cystic fibrosis patients2001 Human biology 73 (3): 403-9
  • Ann Harris
  • Giselda M. K. Cabello
  • Juan Llerena jr
  • Octavio Fernandes
  • Pedro H. Cabello
0018-7143
The selective advantage of cystic fibrosis heterozygotes tested by a DNA analysis: a preliminary investigation2000 International journal of anthropology 15 (3/4): 255-62
  • B. Bramanti
  • B. Chiarelli
  • B. Herrmann
  • D. Caramelli
  • L. Sineo
  • S. Hummel
Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil1999 Human biology 71 (2): 189-96
  • Abilio Santa Rosa
  • Adriana F. Moreira
  • Dafne Horovitz
  • Giselda M. K. Cabello
  • Patrícia Correia
Relationship between genetic anomalies of different levels and deviations in dermatoglyphic traits (5): dermatoglyphic peculiarities of males and females with cystic fibrosis. Family study1999 Zeitschrift für Morphologie und Anthropologie 82 (2/3): 249-302
  • Eugene Kobyliansky
  • Konstantin IAkovenko
  • Mariassa Bat-Miriam Katznelson
  • Michal Bejerano
German summary
Geographic heterogeneity of 4 common worldwide Cystic Fibrosis non-DF508 mutations in Brazil1999 Human biology 71 (1): 111-21
  • Cindy Vnencak-Jones
  • Gail Kaplan
  • John A. Phillips
  • Melodie McClurie
  • Salmo Raskin
The cystic fibrosis heterozygote advantage: a synthesis of ideas1997 Anthropologica (New Series) 39 (1/2): 147-58
  • Kristen M. Beckett
French summary
Étude du retard staturo-pondéral à la naissance chez les enfants attents de mucoviscidose au Saguenay Lac-Saint-Jean (Québec, Canada)1997 Annuaire roumain d'anthropologie 34: 81-7
  • Fernand Simard
  • Gervais Aubin
  • Marc de Braekeleer
H6/HB [ANNUAIRE-]
Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19 /XV-2C haplotype distribution1997 Human biology 69 (4): 499-508
  • Salmo Raskin
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients1993 Human heredity 43 (5): 295-300
  • M P Audrézet
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy1993 Nature 362: 250-5
  • S C Hyde
A more detailed map of the cystic fibrosis mutation DF508 frequencies in Europe1993 Human biology 65 (3): 503-7
  • F Loirat
  • G Lucotte
Cystic fibrosis: sickly channels in mild disease [comments on DN Sheppard and others, see below]1993 Nature 362: 106
  • Christopher Miller
Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties [with comments by C Miller, see above]1993 Nature 362: 160-4
  • D N Sheppard
Cystic fibrosis: vehicles for gene therapy1993 Nature 365: 691-2
  • J M Wilson
Cystic fibrosis: another protein out in the cold [comments on GM Denning and others, see below]1992 Nature 358: 709-10
  • John Armstrong
Advantages of a two-step laboratory approach for cystic fibrosis carrier screening1992 American Journal of human genetics 50 (2): 439-40
  • A L Beaudet
  • W E O'Brien
General population screening for cystic fibrosis is premature1992 American Journal of human genetics 50 (2): 438-9
  • L Biesecker
Spatial distribution of the DF508 mutation in cystic fibrosis: a review1992 Human biology 64 (2): 167-74
  • J Daigneault
  • M de Braekeleer
Cystic fibrosis: a welcome animal model [see also Wilson and Collins, below]1992 Nature 358: 708-9
  • F S Collins
  • J M Wilson
Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians1992 American Journal of human genetics 50 (6): 1185-94
  • G R Cutting
Incidence of cystic fibrosis in Saguenay-Lac-St.-Jean (Quebec, Canada)1992 Human biology 64 (1): 115-19
  • J Daigneault
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive [with comments by J Armstrong, see above]1992 Nature 358: 761-4
  • G M Denning
Cystic fibrosis in the mouse by targeted insertional mutagenesis [with comments by JM Wilson and FS Collins, see below]1992 Nature 359: 211-15
  • J R Dorin
Defective regulation of outwardly rectifying C1 channels by protein kinase A corrected by insertion of CFTR [with comments by C Higgins, see below]1992 Nature 358: 581-4
  • M Egan
Identification of a nonframeshift 84-bp deletion in exon 13 of the cystic fibrosis gene1992 American Journal of human genetics 50 (5): 1022-6
  • R Granell
Cystic fibrosis: chloride channels revisited [comments on M Egan and others, see above]1992 Nature 358: 536
  • C F Higgins
Genetic determination of exocrine pancreatic function in cystic fibrosis1992 American Journal of human genetics 50 (6): 1178-84
  • P Kristidis
The protein kinase A-regulated cardiac CI- channel resembles the cystic fibrosis transmembrane conductance regulator1992 Nature 360: 81-4
  • G Nagel
The cystic fibrosis F508 mutation in the Albanian population1992 American Journal of human genetics 50 (4): 875-6
  • G Novelli
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentation1992 American Journal of human genetics 50 (5): 1140-2
  • V Nunes
Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding [with comments by JJ Wine and SC Silverstein, see below]1992 Nature 360: 79-81
  • M M Reddy
  • P M Quinton
Attitudes toward the prenatal diagnosis of cystic fibrosis: factors in decision making among affected families1992 American Journal of human genetics 50 (5): 1077-85
  • D C Wertz
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