The Effect of Strict Segregation on Pseudomonas aeruginosa in Cystic Fibrosis Patients by van Mansfeld, Rosa, de Vrankrijker, Angelica, Brimicombe, Roland, Heijerman, Harry, Teding van Berkhout, Ferdinand, Spitoni, Cristian, Grave, Sanne, van der Ent, Cornelis, Wolfs, Tom, Willems, Rob, Bonten, Marc

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Chronic obstructive pulmonary disease is not a risk factor for polyneuropathy: A prospective controlled study by Visser, Nora A, Notermans, Nicolette C, Teding van Berkhout, Ferdinand, van den Berg, Leonard H, Vrancken, Alexander FJE

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Body Weight and Body Mass Index in Patients with End-Stage Cystic Fibrosis Stabilize After the Start of Enteral Tube Feeding by Hollander, Francis M., de Roos, Nicole M., Belle van Meerkerk, Gerdien, Teding van Berkhout, Ferdinand, Heijerman, Harry G.M., van de Graaf, Ed A.

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Pseudomonas aeruginosa Genotype Prevalence in Dutch Cystic Fibrosis Patients and Age Dependency of Colonization by Various P. aeruginosa Sequence Types by VAN MANSFELD, Rosa, WILLEMS, Rob, BRIMICOMBE, Roland, HEIJERMAN, Harry, VAN BERKHOUT, Ferdinand Teding, WOLFS, Tom, VAN DER ENT, Cornelis, BONTEN, Marc

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Pseudomonas aeruginosa Genotype Prevalence in Dutch Cystic Fibrosis Patients and Age Dependency of Colonization by Various P. aeruginosa Sequence Types by van Mansfeld, Rosa, Willems, Rob, Brimicombe, Roland, Heijerman, Harry, Teding van Berkhout, Ferdinand, Wolfs, Tom, van der Ent, Cornelis, Bonten, Marc

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Schwannoma of the Recurrent Laryngeal Nerve: A Rare Entity by de Heer, Linda M., van Berkhout, Ferdinand Teding, Priesterbach-Ackley, Loudy P., Buijsrogge, Marc P.

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Outcome of assisted ventilation for acute respiratory failure in cystic fibrosis by SLIEKER, Martijn G, VAN GESTEL, Josephus P. J, HEIJERMAN, Harry G. M, TRAMPER-STRANDERS, Gerdien A, VAN BERKHOUT, Ferdinand Teding, VAN DER ENT, Cornelis K, JANSEN, Nicolaas J. G

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Schwannoma of the Recurrent Laryngeal Nerve: A Rare Entity by de Heer, Linda M., van Berkhout, Ferdinand Teding, Priesterbach-Ackley, Loudy P., Buijsrogge, Marc P.

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Long-term effects of birth order and age at diagnosis in cystic fibrosis: A sibling cohort study by Slieker, M.G., van den Berg, J.M.W., Kouwenberg, J., van Berkhout, F. Teding, Heijerman, H.G.M., van der Ent, C.K.

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Assessment of nutritional status in adult patients with cystic fibrosis: Whole-body bioimpedance vs body mass index, skinfolds, and leg-to-leg bioimpedance by Hollander, Francis M., de Roos, Nicole M., de Vries, Jeanne H.M., van Berkhout, Ferdinand Teding

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