Zoekresultaten - William van’t Hoff

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  1. 1
    The effect of hypopituitarism on life expectancy.

    The effect of hypopituitarism on life expectancy. door Andrew Bates, William van’t Hoff, Peter J.H. Jones, R. N. Clayton

    Gepubliceerd in 1996
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  2. 2
    The orthopaedic management of lower limb deformity in hypophosphataemic rickets

    The orthopaedic management of lower limb deformity in hypophosphataemic rickets door A Horn, Jonathan Wright, Detlef Böckenhauer, William van’t Hoff, Deborah M. Eastwood

    Gepubliceerd in 2017
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  3. 3
    Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK

    Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK door Naomi Issler, Stephanie Dufek, Robert Kleta, Detlef Böckenhauer, Naima Smeulders, William van’t Hoff

    Gepubliceerd in 2017
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  4. 4
    Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases

    Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases door Detlef Böckenhauer, William van’t Hoff, Mehul Dattani, A. Lehnhardt, M.S. Subtirelu, Friedhelm Hildebrandt, Daniel G. Bichet

    Gepubliceerd in 2010
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  5. 5
    Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin

    Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin door Marlene Attard, G Jean, Lionel Forestier, Stéphanie Cherqui, William van’t Hoff, M. Broyer, Corinne Antignac, M Town

    Gepubliceerd in 1999
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  6. 6
    Bi‐allelic <i>CLPB</i> mutations cause cataract, renal cysts, nephrocalcinosis and 3‐methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation

    Bi‐allelic <i>CLPB</i> mutations cause cataract, renal cysts, nephrocalcinosis and 3‐methylglutaconic aciduria, a novel disorder of mitochondrial protein disaggregation door Marta Kanabus, Rojeen Shahni, José W. Saldanha, Elaine Murphy, Vincent Plagnol, William van’t Hoff, Simon Heales, Shamima Rahman

    Gepubliceerd in 2015
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  7. 7
    Renal Phenotype in Lowe Syndrome

    Renal Phenotype in Lowe Syndrome door Detlef Böckenhauer, Arend Bökenkamp, William van’t Hoff, Elena Levtchenko, Joana E. Kist‐van Holthe, Velibor Tasic, Michael Ludwig

    Gepubliceerd in 2008
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  8. 8
    Novel OCRL mutations in patients with Dent-2 disease

    Novel OCRL mutations in patients with Dent-2 disease door Detlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, Robert J. Unwin, William van’t Hoff, Tony Sirimanna, Kristina Vrljičak, Michael Ludwig

    Gepubliceerd in 2015
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  9. 9
    Sleep apnoea in acromegaly.

    Sleep apnoea in acromegaly. door W H Perks, P.M. Horrocks, R. Cooper, Sarah Bradbury, Angier Allen, N.M. Baldock, K Prowse, William van’t Hoff

    Gepubliceerd in 1980
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  10. 10
    Molecular Characterization of CTNS Deletions in Nephropathic Cystinosis: Development of a PCR-Based Detection Assay

    Molecular Characterization of CTNS Deletions in Nephropathic Cystinosis: Development of a PCR-Based Detection Assay door Lionel Forestier, G Jean, Marlene Attard, Stéphanie Cherqui, Cathryn M. Lewis, William van’t Hoff, M. Broyer, Margaret Town, Corinne Antignac

    Gepubliceerd in 1999
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  11. 11
    Clinical and diagnostic features of Bartter and Gitelman syndromes

    Clinical and diagnostic features of Bartter and Gitelman syndromes door Patrick R. Walsh, Yincent Tse, Emma Ashton, Daniela Iancu, Lucy Jenkins, Marc Bienias, Robert Kleta, William van’t Hoff, Detlef Böckenhauer

    Gepubliceerd in 2017
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  12. 12
    Guidance on clinical research involving infants, children and young people: an update for researchers and research ethics committees

    Guidance on clinical research involving infants, children and young people: an update for researchers and research ethics committees door Neena Modi, J. Vohra, Jennifer Preston, Christina Elliott, William van’t Hoff, Jane Coad, Faith Gibson, Linda Partridge, Joe Brierley, Vic Larcher, Anne Greenough

    Gepubliceerd in 2014
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  13. 13
    Ergocalciferol Supplementation in Children with CKD Delays the Onset of Secondary Hyperparathyroidism

    Ergocalciferol Supplementation in Children with CKD Delays the Onset of Secondary Hyperparathyroidism door Rukshana Shroff, Mandy Wan, Ambrose Gullett, Sarah Ledermann, Rachel Shute, Craig Knott, David G. Wells, Helen Aitkenhead, Bahee Manickavasagar, William van’t Hoff, Lesley Rees

    Gepubliceerd in 2012
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  14. 14
    Hypervitaminosis A is prevalent in children with CKD and contributes to hypercalcemia

    Hypervitaminosis A is prevalent in children with CKD and contributes to hypercalcemia door Baheerathi Manickavasagar, Andrew McArdle, Pallavi Yadav, Vanessa Shaw, Marjorie Dixon, Rune Blomhoff, Graeme O’ Connor, Lesley Rees, Sarah Ledermann, William van’t Hoff, Rukshana Shroff

    Gepubliceerd in 2014
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  15. 15
    Standard 1: Consent and Recruitment

    Standard 1: Consent and Recruitment door Patrina Caldwell, Leonila F. Dans, Martine C. de Vries, Jenny Newman, Helen Sammons, Merle Spriggs, Parag Tambe, William van’t Hoff, Kerry Woolfall, Bridget Young, Martin Offringa

    Gepubliceerd in 2012
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  16. 16
    Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked Hypophosphatemia

    Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked Hypophosphatemia door Agnès Linglart, Erik A. Imel, Michael P. Whyte, Anthony A. Portale, Wolfgang Högler, Annemieke M. Boot, Raja Padidela, William van’t Hoff, Gary S. Gottesman, Angel Chen, Alison Skrinar, Mary Scott Roberts, Thomas O. Carpenter

    Gepubliceerd in 2021
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  17. 17
    Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome

    Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome door Dorothy Thompson, Sally Feather, Horia Stanescu, Bernard Freudenthal, Anselm A. Zdebik, Richard Warth, Miloš Ognjanović, Sally A. Hulton, Evangeline Wassmer, William van’t Hoff, Isabelle Russell‐Eggitt, Angus Dobbie, Eamonn Sheridan, Robert Kleta, Detlef Böckenhauer

    Gepubliceerd in 2011
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  18. 18
    Burosumab Therapy in Children with X-Linked Hypophosphatemia

    Burosumab Therapy in Children with X-Linked Hypophosphatemia door Thomas O. Carpenter, Michael P. Whyte, Erik A. Imel, Annemieke M. Boot, Wolfgang Högler, Agnès Linglart, Raja Padidela, William van’t Hoff, Meng Mao, Chao-Yin Chen, Alison Skrinar, Emil Kakkis, Javier San Martín, Anthony A. Portale

    Gepubliceerd in 2018
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  19. 19
    Conservative treatment for uncomplicated appendicitis in children: the CONTRACT feasibility study, including feasibility RCT

    Conservative treatment for uncomplicated appendicitis in children: the CONTRACT feasibility study, including feasibility RCT door Nigel Hall, Frances Sherratt, Simon Eaton, Isabel Reading, Erin Walker, Maria Chorozoglou, Lucy Beasant, Wendy Wood, Michael Stanton, Harriet J. Corbett, Dean Rex, Natalie Hutchings, Elizabeth Dixon, Simon Grist, William van’t Hoff, Esther Crawley, Jane Blazeby, Bridget Young

    Gepubliceerd in 2021
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  20. 20
    Acidosis and Deafness in Patients with Recessive Mutations in FOXI1

    Acidosis and Deafness in Patients with Recessive Mutations in FOXI1 door Sven Enerbäck, Daniel Nilsson, Noel Edwards, Mikael Heglind, Sumaya Alkanderi, Emma Ashton, Asma Deeb, Feras E.B. Kokash, Abdul Rahim Ali Bakhsh, William van’t Hoff, Stephen B. Walsh, Felice D’Arco, Arezoo Daryadel, Soline Bourgeois, Carsten A. Wagner, Robert Kleta, Detlef Böckenhauer, John A. Sayer

    Gepubliceerd in 2017
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