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Title	Date	Reference	Authors	Call #	ISSN
The weariness of hoping: synchronizing affect while awaiting organ transplantation for cystic fibrosis in Germany	2023	Medical anthropology 42 (6): 593-606	Carsten Schwarz Jörg Niewöhner Stefan Reinsch	H6/KGT [MEDICAL-]	1545-5882
Therapeutic endings: reflections of counselling-based research relationships among patients with cystic fibrosis and their caregivers	2019	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 illness	2018	Curare 41 (1-2): 115-33, 168, 175	Doris Staab Jörg Niewöhner Stefan Reinsch	H6/KGT [CURARE-]	0344-8622
When care strikes back - some strategies and tactics for dealing with ambivalence of visibility in chronic illness	2016	Irish journal of anthropology 19 (1): 82-90	Doris Staab Jörg Niewöhner Stefan Reinsch	H6/KVC [IRISH-]	1393-8592
Ambivalent visibility: chronic illness and image in young adulthood	2015	Medicine Anthropology Theory 2 (3): 168-77	Johannes Rascher Stefan Reinsch		2405-691X
Association of CFTR gene mutation with bronchial asthma and its severity in Indian children: a case-control study	2012	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 Africa	2012	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 population	2011	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 fibrosis	2008	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, Brazil	2007	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 fibrosis	2006	Česká antropologie 56 (): 145-8	Eva Nešćáková Hana Kayserova Milica Beránková Paula Zajacova Stanislav Katina Zuzana Kapustova	H6/KVL [ANTROPOLOGICKÁ-]	0862-5085
Sequence of ΔF 508 CFTR allele identified at present is lacking in medieval specimens from central Poland. Preliminary results	2006	Anthropologischer Anzeiger 64 (1): 41-9	Anna Wrzesińska Elżbieta Żądzińska Henryk W. Witas Izabela Jatczak Krystyna Jędrychowska-Dańska	H6/HB [ANTHROPOLOGISCHER-]	0003-5548
Molecular analysis of 23 exons of the CFTR gene in Brazilian patients leads to the finding of rare cystic fibrosis mutations	2005	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 screening	2005	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 fibrosis	2005	Przegląd antropologiczny 68 (): 53-64	Anita Szwed Joachim Cieślik Joanna Goździk Karol Karbowy Magdalena Kosińska	H6/KE [PRZEGLAD-]	0033-2003
What is incidence of cystic fibrosis in Italy ? Data from the National Registry	2004	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 Rica	2003	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, Brazil	2003	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
The 3120 +1G→A splicing mutation in CFTR is common in Brazilian cystic fibrosis patients	2001	Human biology 73 (3): 403-9	Ann Harris Giselda M. K. Cabello Juan Llerena jr Octavio Fernandes Pedro H. Cabello		0018-7143
Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients	2001	Human biology 73 (2): 191-203	Hulya Kayseruku Julian Zielenski Nalan Gokgoz Ozlem Topaloglu Tuncer Onay		0018-7143
The selective advantage of cystic fibrosis heterozygotes tested by a DNA analysis: a preliminary investigation	2000	International journal of anthropology 15 (3/4): 255-62	B. Bramanti B. Chiarelli B. Herrmann D. Caramelli L. Sineo S. Hummel
Geographic heterogeneity of 4 common worldwide Cystic Fibrosis non-DF508 mutations in Brazil	1999	Human biology 71 (1): 111-21	Cindy Vnencak-Jones Gail Kaplan John A. Phillips Melodie McClurie Salmo Raskin
Relationship between genetic anomalies of different levels and deviations in dermatoglyphic traits (5): dermatoglyphic peculiarities of males and females with cystic fibrosis. Family study	1999	Zeitschrift für Morphologie und Anthropologie 82 (2/3): 249-302	Eugene Kobyliansky Konstantin IAkovenko Mariassa Bat-Miriam Katznelson Michal Bejerano
Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil	1999	Human biology 71 (2): 189-96	Abilio Santa Rosa Adriana F. Moreira Dafne Horovitz Giselda M. K. Cabello Patrícia Correia
Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19 /XV-2C haplotype distribution	1997	Human biology 69 (4): 499-508	Salmo Raskin
The cystic fibrosis heterozygote advantage: a synthesis of ideas	1997	Anthropologica (New Series) 39 (1/2): 147-58	Kristen M. Beckett
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: vehicles for gene therapy	1993	Nature 365 (): 691-2	J M Wilson
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: sickly channels in mild disease [comments on DN Sheppard and others, see below]	1993	Nature 362 (): 106	Christopher Miller
A more detailed map of the cystic fibrosis mutation DF508 frequencies in Europe	1993	Human biology 65 (3): 503-7	F Loirat G Lucotte
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy	1993	Nature 362 (): 250-5	S C Hyde
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients	1993	Human heredity 43 (5): 295-300	M P Audrézet
Cystic fibrosis: ATP and chloride conductance [comments on PM Quinton and MM Reddy, see above]	1992	Nature 360 (): 18	J J Wine S C Silverstein
Cystic fibrosis: another protein out in the cold [comments on GM Denning and others, see below]	1992	Nature 358 (): 709-10	John Armstrong
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
Advantages of a two-step laboratory approach for cystic fibrosis carrier screening	1992	American Journal of human genetics 50 (2): 439-40	A L Beaudet W E O'Brien
General population screening for cystic fibrosis is premature	1992	American Journal of human genetics 50 (2): 438-9	L Biesecker
Spatial distribution of the DF508 mutation in cystic fibrosis: a review	1992	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 Caucasians	1992	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
Cystic fibrosis: more from the modellers [comments on JR Dorin and others, see above; see also Collins and Wilson, above]	1992	Nature 359 (): 195-6	F S Collins J M Wilson
Identification of a nonframeshift 84-bp deletion in exon 13 of the cystic fibrosis gene	1992	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 fibrosis	1992	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 regulator	1992	Nature 360 (): 81-4	G Nagel

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Anthropological Index Online