Pronađeno 40 radova, za izraz:
"PROJEKT: (Genetika, priroda i epidemiologija značajnijih živčanih i mišićnih bolesti (ŽMB) (MZOS-108-0000000-3435))"
DODAJ/IZMIJENI OPERATORE PRETRAŽIVANJA
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26.Canki-Klain, NinaGenetsko testiranje monogenskih bolesti // Biochemia medica 19/Suppl 1
Zagreb, 2009. str. S46-S46 (pozvano predavanje, domaća recenzija, sažetak, znanstveni) -
27.Canki-Klain, Nina; Beroud, Christophe; Clarke Nigel F.; Kovač, Ida; Chambert, Sophie; Guicheney PascaleThe adult phenotype of congenital muscular dystrophy (MDC1A) due to mutation of LAMA2 // Neuromuscular Disorders 19 (2009) (8/9) 511-674 Abstracts of the 14th International Congress of the World Muscle Society
Švicarska, 2009. str. 574-574 (poster, međunarodna recenzija, sažetak, znanstveni) -
28.Canki-Klain, NinaThe impact of molecular diagnosis on management and counseling in prevalent Mendelian muscle and nerve disorders // NEUROMEDITERRANEAN 10
Durres: "EDLORA", 2009. str. 14-14 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni) -
29.Žagar, MarijaNeuromuskularne bolesti // Interna medicina (četvrto promjenjeno i dopunjeno izdanje) / Vrhovac, Božidar ; Jakšić, Branimir ; Reiner, Željko, Vucelić, Boris (ur.).
Zagreb: Naklada Ljevak, 2008. str. 1587-1591 -
30.CANKI-KLAIN, Nina; PAVLIN, Katarina; AVANZO-VELKAVRH Mariija(Ljubljana , Slovenia), AUDREZET, Marie-Pierrre; FEREC, Claude (Brest, France)NEONATAL SCREENING FOR CYSTIC FIBROSIS USING IMMUNOREACTIVE TRYPSINOGEN AND DIRECT GENE ANALYSIS IN SLOVENIA // "What's New in the Diagnosis, Treatment and Prevention of Cystic Fibrosis?" First Eastern European CF Conference / Canki-Klain, Nina ; Kovačić, Sanja (ur.).
Zagreb: Medicinska knjiga, 2008. str. 44-44 (predavanje, međunarodna recenzija, sažetak, znanstveni) -
31.Canki-Klain, Nina, Kovačić, Sanja(ur.)"What's new in diagnosis, treatment and prevention of cystic fibrosis?" First Eastern European Conference. Zagreb: Medicinska knjiga, 2008 (monografija)
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32.Canki-Klain.NinaThe impact of molecular diagnosis on management and counselling in major inherited neuromuscular disorders // OMICS In The 21st Century.Fifth International Symposium on Genetics, Health and Disease
Amritsar: Guru Nanak Dev University, Amritsar, India, 2008. str. 8-8 (pozvano predavanje, međunarodna recenzija, sažetak, ostalo) -
33.Canki-Klain, Nina, Žagar, Marija, Lannoy N, Verellen-Dumoulin, ChristinePossible Mechanims Responsible for great Inter and Intra Familial Phenotypic Heterogeneity in FSHD // Facioscapulohumeral Muscular Dystrophy [FSHD] International Research Consortium 2008 Tuesday, November 11, 2008 7:30 a.m. – 5:00 p.m. Philadelphia Marriott® ; Downtown 1201 Market Street, Philadelphia, Pennsylvania 19107 USA Salons A and B / Daniel Paul Perez, Kathryn Wagner, M.D., Ph.D., Silvè ; re van der Maarel, Ph.D. (ur.).
Watertown (MA): FSH Society, USA, AFM, NIH, 2008. str. 27-28 (pozvano predavanje, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni) -
34.Canki-Klain.Nina, Lessel, DavorPraktički aspekti genetskog savjetovanja / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, Kranjčevićeva 25, Zagreb, 2007 -
35.Milić, AstridPRAKTIČKI ASPEKTI GENETSKOG SAVJETOVANJA / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, Kranjčevićeva 25, Zagreb, 2007 -
36.Canki-Klain, NinaPRAKTIČKI ASPEKTI GENETSKOG SAVJETOVANJA / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, Kranjčevićeva 25, Zagreb, 2007 -
37.Canki-Klain, Nina; Quijano-Roy, Susana; Antun Sasso; Telarović, Srđana; Lessel, Davor; Stiglmayer, Neda; Juri, Jelena; Žagar, Marija; Gjergja, Romana; Stipoljev, Feodora et al.PRAKTIČKI ASPEKTI GENETSKOG SAVJETOVANJA / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, Kranjčevićeva 25, Zagreb, 2007 -
38.Lessel, Davor; Canki-Klain, Nina; Hečimović, Silva; Radoš, MarkoProgression of Juvenile Huntington's Disease (JGH) with Dysarthrophonia as Presenting Symptom:A Case Report // World Congress on Huntington's Disease, HD 2007, Dresden, Germany, September 8-11, 2007, Final Programme and Abstracts
Dresden, 2007. str. 114-115 (poster, međunarodna recenzija, sažetak, ostalo) -
39.Canki-Klain, Nina; Žagar, Marija; Alfirević –Ungarov, Tajda; Milić, Astrid; Malnar, Martina; Mitrović, Zoran; Vranješ, Davorka; Kovač, Biserka; Cvitanović-Šojat, LjerkaClinical, genetic and epidemiological study of prevalent autosoma recessive limb girdle muscular dystrophies in Croatia // Programme and Abstracts of the 12th International Congress of the World Muscle Society ; u: Neuromuscular disorders 17 (2001) (9/10) 810-811
Taormina, Italija, 2007. str. 810-811 (poster, sažetak, znanstveni) -
40.Canki-Klain, Nina; Bošnjak, Ivan; Kvakić, Milka; Sepčić, Juraj; Marković, Dubravko; Gjergja Juraški, Romana; Jokić-Begić, Nataša; Stipoljev, Feodora; Lessel, Davor; Vranješ, Davorka et al.Praktični aspekti genetskog savjetovanja / Canki-Klain, Nina (ur.).
Zagreb: COPY SERVIS, 2007