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Items: 5

1.

Volatile organic compound breath signatures of children with cystic fibrosis by real-time SESI-HRMS.

Weber R, Haas N, Baghdasaryan A, Bruderer T, Inci D, Micic S, Perkins N, Spinas R, Zenobi R, Moeller A.

ERJ Open Res. 2020 Jan 10;6(1). pii: 00171-2019. doi: 10.1183/23120541.00171-2019. eCollection 2020 Jan.

PMID:
31956658
2.

Images in clinical medicine. Aquagenic wrinkling of palms in cystic fibrosis.

Weibel L, Spinas R.

N Engl J Med. 2012 May 24;366(21):e32. doi: 10.1056/NEJMicm1103833. No abstract available.

3.

Large deletions in the CFTR gene: clinics and genetics in Swiss patients with CF.

Schneider M, Hirt C, Casaulta C, Barben J, Spinas R, Bühlmann U, Spalinger J, Schwizer B, Chevalier-Porst F, Gallati S.

Clin Genet. 2007 Jul;72(1):30-8.

PMID:
17594397
4.

Sweat testing practice in Swiss hospitals.

Barben J, Casaulta C, Spinas R, Schöni MH; Swiss Working Group for Cystic Fibrosis (SWGCF).

Swiss Med Wkly. 2007 Apr 7;137(13-14):192-8.

PMID:
17525871
5.

Acidic fibroblast growth factor (aFGF) is present in the fluid of brain tumour pseudocysts.

Moringlane JR, Spinas R, Böhlen P.

Acta Neurochir (Wien). 1990;107(3-4):88-92.

PMID:
1706557

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