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51

Bone marrow transplantation for Maroteaux–Lamy syndrome (MPS VI): Long-term follow-up

E. Herskhovitz, E. Young, J. Rainer, C. M. Hall, V. Lidchi, K. Chong, A. Vellodi

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 133 KB

english, 1999

52

Long-term follow-up following bone marrow transplantation for Hunter disease

A. Vellodi, E. Young, A. Cooper, V. Lidchi, B. Winchester, J. E. Wraith

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 81 KB

english, 1999

53

Protein, glucose and energy metabolism in Gaucher disease type I

O. A. F. Bodamer, A. Vellodi

Journal:

Journal of Inherited Metabolic Disease

Year:

2000

Language:

english

File:

PDF, 32 KB

english, 2000

54

Failure of tumor-reactive lymph node cells to kill tumor in the presence of immune-suppressive CD34+cells can be overcome with vitamin D3treatment to diminish CD34+cell levels

Kristina Wiers, Mark A. Wright, Kishore Vellody, M. Rita I. Young

Journal:

Clinical and Experimental Metastasis

Year:

1998

Language:

english

File:

PDF, 537 KB

english, 1998

55

Management of neuronopathic Gaucher disease: A European consensus

A. Vellodi, B. Bembi, T.B. de Villemeur, T. Collin-Histed, A. Erikson, E. Mengel, A. Rolfs, A. Tylki-Szymanska

Journal:

Journal of Inherited Metabolic Disease

Year:

2001

Language:

english

File:

PDF, 75 KB

english, 2001

56

Safety and Efficacy of Enzyme Replacement Therapy with Agalsidase Beta: An International, Open-label Study in Pediatric Patients with Fabry Disease

J. Edmond Wraith, Anna Tylki-Szymanska, Nathalie Guffon, Y. Howard Lien, Michel Tsimaratos, Ashok Vellodi, Dominique P. Germain

Journal:

The Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 198 KB

english, 2008

57

P05.10 Early-onset Gaucher disease (GD) in an infant – what phenotype to expect along the neuronopathic continuum and how to treat it?

M. Ćuk, K. Fumić, K. Bilić, E. Sidransky, A. Vellodi, K. Juras, V. Sarnavka, L. Jelinić, L.J. Rajić, M. Mikulić, R. Stern Padovan, M. Čačić Hribljan, T. Matić, M. Cvitković, S. Galić, M. Novak, D. Ric

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 54 KB

english, 2011

58

Is globotriaosylceramide a useful biomarker in Fabry disease?

E Young, K Mills, P Morris, A Vellodi, P Lee, S Waldek, B Winchester

Journal:

Acta Paediatrica

Year:

2005

Language:

english

File:

PDF, 54 KB

english, 2005

59

Ultrastructural Study of the Cornea in a Bone Marrow-Transplanted Hurler Syndrome Patient

Y. HUANG, A.J. BRON, K.M. MEEK, A. VELLODI, B. McDONALD

Journal:

Experimental Eye Research

Year:

1996

Language:

english

File:

PDF, 4.64 MB

english, 1996

60

Gaucher disease in children: radiology of non-central nervous system manifestations

K McHugh, Ø.E Olsen, A Vellodi

Journal:

Clinical Radiology

Year:

2004

Language:

english

File:

PDF, 2.00 MB

english, 2004

61

The normal distribution of thoracoabdominal aorta small branch artery ostia

Paul Cronin, David M. Williams, Ranjith Vellody, Aine Marie Kelly, Ella A. Kazerooni, Ruth C. Carlos

Journal:

European Journal of Radiology

Year:

2011

Language:

english

File:

PDF, 565 KB

english, 2011

62

39 Formation of a Lysosomal Disease Testing Network to enhance the delivery of diagnostic services to patients with lysosomal storage disorders

Christine Eng, J. Muenzer, E. Wraith, M. Beck, R. Giugliani, P. Harmatz, A. Vellodi, R. Martin, U. Ramaswami, M. Calikoglu, S. Vijayaraghavan, A. Puga, B. Ulbrich, M. Shinawi, M. Cleary, S. Wendt

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 44 KB

english, 2007

63

29 Clinical benefit of enzyme replacement therapy (ERT) in mucopolysaccharidosis II (MPS II, Hunter syndrome)

Christine Eng, J. Muenzer, E. Wraith, M. Beck, R. Giugliani, P. Harmatz, A. Vellodi, R. Martin, U. Ramaswami, M. Calikoglu, S. Vijayaraghavan, A. Puga, B. Ulbrich, M. Shinawi, M. Cleary, S. Wendt

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

64

107 Two-year oral miglustat in Gaucher disease type III

Raphael Schiffmann, Harris Chris, DeVile Catherine, Davis-Pope Elin, Fitzgibbon Ed, Brady Roscoe, Abel Larry, Campbell Pauline, Vellodi Ashok

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

65

35. Guidelines for the assessment and monitoring of bone disease in children with Gaucher disease

Gregory A. Grabowski, Thomas Hangartner, Paige Kaplan, Mario Maas, Giuliano Mariani, Kieran McHugh, Sheila Moore, Ashok Vellodi, John Yee, Lynne Steinbach

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 57 KB

english, 2008

66

110. Changes in gait pattern as assessed by the GaitRite walkway system in MPS II patients undergoing enzyme replacement therapy

Michelle Wood, Ashok Vellodi

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 43 KB

english, 2008

67

54. Clinical and demographic characteristics of 131 patients with neuronopathic Gaucher disease enrolled in the Neurological Outcomes Sub-Registry of the ICGG Gaucher Registry

Edwin Kolodny, Ashok Vellodi, Amal El-Beshlawy, J. Alexander Cole, Anna Tylki-Szymanski

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 43 KB

english, 2008

68

31. Girls just want to have fun!

Niamh Finnegan, Ashok Vellodi, Elin Davies

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 54 KB

english, 2008

69

109. Observed changes in behaviour with assessment and procedures in neurologically affected boys with mucopolysaccharidosis type II undergoing enzyme replacement therapy

Michelle Wood, Niamh Finnegan, Ashok Vellodi

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 56 KB

english, 2008

70

Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometry

Clare E. Beesley, Elisabeth P. Young, Niamh Finnegan, Marie Jackson, Kevin Mills, Ashok Vellodi, Maureen Cleary, Bryan G. Winchester

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 383 KB

english, 2009

71

149. Avascular Necrosis in type I Gaucher disease: Analysis of risk factors

Neal Weinreb, Patrick Deegan, Ashok Vellodi, J. Alexander Cole, Michael Yeh, Pramod Mistry

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

72

Defining the Gait profile of children with Neuronopathic Gaucher disease

Elin Davies, Lucy Alderson, Michelle Wood, Ashok Vellodi

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 58 KB

english, 2011

73

Diffusion tensor imaging: Study of white-matter brain in paediatric patients with Gaucher disease

Elin Davies, Kiran Seunarine, Chris Clark, Vellodi Ashok

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 58 KB

english, 2011

74

Behavioural aspects of Gaucher's disease – An explorative study

Lauren McPartlan, Ruksana Ahmed, Ashok Vellodi, Paramala Santosh

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 77 KB

english, 2011

75

Laboratory Investigation of Pompe Disease

Katie Bainbridge, Derek Burke, Vicki Manwaring, Helen Prunty, Ashok Vellodi, Simon Heales

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 54 KB

english, 2012

76

Long Term Outcomes of a Phase 1/2, Multicenter, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Efficacy of BMN 110 in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome)

Christian Hendriksz, Ashok Vellodi, Simon Jones, Hiwot Takkele, S. Lee, Sarah Chesler, Celeste Decker

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 57 KB

english, 2012

77

Combination of Enzyme Replacement Therapy and Hematopoietic Stem Cell Transplantation among MPS I Patients: An MPS I Registry Analysis

Kristin D'Aco, Edmond Wraith, Chester Whitley, Fritz Wijburg, Ashok Vellodi, Rossella Parini, Paige Kaplan, Heather Stein, Lakshmi Rangachari, Gerald Cox

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 56 KB

english, 2012

78

Phenotypic Spectrum of Hematological and Visceral Disease in Type 3 Gaucher Disease and Response to Imiglucerase Therapy: Preliminary Analysis from the ICGG Gaucher Registry

Pramod Mistry, Edwin Kolodny, Anna Tylki-Szymanska, Nadia Belmatoug, Juan Cabello, Ashok Vellodi, J. Alexander Cole, Gregory Grabowski

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 66 KB

english, 2012

79

BMN 110 (Recombinant Human GALNS), an Investigational Enzyme Replacement Therapy for Mucopolysaccharidosis Type IVA (MPS IVA Or Morquio Syndrome), Promotes Type II Collagen Synthesis in MPS IVA Patients

Florence Lorget, Sungwook Lee, Kelly Lau, Laurie Tsuruda, Chris Hendriksz, Simon Jones, Ashok Vellodi, Sabrina cheng, Celeste Decker, Charles O'Neill

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 55 KB

english, 2012

80

Bone marrow transplantation for autosomal recessive osteopetrosis A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group

Egbert J.A. Gerritsen, Jaak M. Vossen, Anders Fasth, Wilhelm Friedrich, Gareth Morgan, Andrew Padmos, Ashok Vellodi, Oscar Porras, Ann O'Meara, Fulvio Porta, Pierre Bordigoni, Andrew Cant, Jo Hermans,

Journal:

The Journal of Pediatrics

Year:

1994

Language:

english

File:

PDF, 614 KB

english, 1994

81

Fabrazyme® therapy in pediatric patients with Fabry disease: Improvements in quality-of-life measures

A. Tylki-Szymanska, D.P. Germain, J.E. Wraith, N. Guffon, Y.H. Lien, M. Tsimaratos, A. Vellodi

Journal:

Clinical Therapeutics

Year:

2007

Language:

english

File:

PDF, 223 KB

english, 2007

82

Disordered breathing during sleep in patients with mucopolysaccharidoses

S.E.J Leighton, B Papsin, A Vellodi, R Dinwiddie, R Lane

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2001

Language:

english

File:

PDF, 107 KB

english, 2001

83

Otologic and laryngologic manifestations of mucopolysaccharidoses after bone marrow transplantation

B.C. Papsin, A. Vellodi, C.M. Bailey, P.C. Ratcliff, S.E.J. Leighton

Journal:

Otolaryngology - Head and Neck Surgery

Year:

1998

Language:

english

File:

PDF, 92 KB

english, 1998

84

Letters to the editor

F.S. Haddad, D.H.A. Jones, A. Vellodi, N. Kane, M. Pitt

Journal:

The Journal of Hand Surgery: British & European Volume

Year:

1996

Language:

english

File:

PDF, 668 KB

english, 1996

85

Protein phosphatase-2A association with microtubules and its role in restricting the invasiveness of human head and neck squamous cell carcinoma cells

Jeremy Meisinger, Snehal Patel, Kishore Vellody, Richard Bergstrom, Janet Benefield, Yvonne Lozano, M.Rita I. Young

Journal:

Year:

1997

Language:

english

File:

PDF, 2.52 MB

english, 1997

86

Carpal tunnel syndrome in children with storage disorders

N.M. Kane, F.S. Haddad, M.C. Fitt, A. Vellodi, D.H.A. Jones

Journal:

Electroencephalography and Clinical Neurophysiology

Year:

1997

Language:

english

File:

PDF, 173 KB

english, 1997

87

Macrophage colony-stimulating factor and receptor activator NF-κB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitro

A.M. Flanagan, H.M. Massey, C. Wilson, A. Vellodi, M.A. Horton, C.G. Steward

Journal:

Year:

2002

Language:

english

File:

PDF, 265 KB

english, 2002

88

Cockroach cause of allergic asthma 1, 2Its specificity and immunologic profile

KANG, B, VELLODY, D, HOMBURGER, H, YUNGINGER, J

Journal:

Journal of Allergy and Clinical Immunology

Year:

1979

Language:

english

File:

PDF, 655 KB

english, 1979

89

Electron Microscopy of Chorionic Villus Samples for Prenatal Diagnosis of Lysosomal Storage Disorders

Fowler, D. J., Anderson, G., Vellodi, A., Malone, M., Sebire, N. J.

Journal:

Ultrastructural Pathology

Year:

2007

Language:

english

File:

PDF, 1.67 MB

english, 2007

90

Type II Gaucher disease manifesting as haemophagocytic lymphohistiocytosis

Sharpe, L.-R., Ancliff, P., Amrolia, P., Gilmour, K. C., Vellodi, A.

Journal:

Journal of Inherited Metabolic Disease

Year:

2009

Language:

english

File:

PDF, 97 KB

english, 2009

91

Changes in gait pattern as assessed by the GAITRite™ walkway system in MPS II patients undergoing enzyme replacement therapy

Wood, M., Cleary, M. A., Alderson, L., Vellodi, A.

Journal:

Journal of Inherited Metabolic Disease

Year:

2009

Language:

english

File:

PDF, 301 KB

english, 2009

92

Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes

Burke, Derek G., Rahim, Ahad A., Waddington, Simon N., Karlsson, Stefan, Enquist, Ida, Bhatia, Kailash, Mehta, Atul, Vellodi, Ashok, Heales, Simon

Journal:

Journal of Inherited Metabolic Disease

Year:

2013

Language:

english

File:

PDF, 121 KB

english, 2013

93

Imaging of Renin-Mediated Hypertension in Children

Castelli, Patricia K., Dillman, Jonathan R., Smith, Ethan A., Vellody, Ranjith, Cho, Kyung, Stanley, James C.

Journal:

American Journal of Roentgenology

Year:

2013

Language:

english

File:

PDF, 1.15 MB

english, 2013

94

Erratum to: Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes

Burke, Derek G., Rahim, Ahad A., Waddington, Simon N., Karlsson, Stefan, Enquist, Ida, Bhatia, Kailash, Mehta, Atul, Vellodi, Ashok, Heales, Simon

Journal:

Journal of Inherited Metabolic Disease

Year:

2013

Language:

english

File:

PDF, 51 KB

english, 2013

95

Magnetic Resonance Angiography of the Pediatric Abdomen and Pelvis

Vellody, Ranjith, Liu, Peter S., Sada, David M.

Journal:

Magnetic Resonance Imaging Clinics of North America

Year:

2013

Language:

english

File:

PDF, 3.40 MB

english, 2013

96

Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis

Pangrazio, Alessandra, Puddu, Alessandro, Oppo, Manuela, Valentini, Maria, Zammataro, Luca, Vellodi, Ashok, Gener, Blanca, Llano-Rivas, Isabel, Raza, Jamal, Atta, Irum, Vezzoni, Paolo, Superti-Furga,

Journal:

Year:

2014

Language:

english

File:

PDF, 447 KB

english, 2014

97

GROUP-A STREPTOCOCCAL INFECTION IN THE NEWBORN

Coulter, J.B.S., Buchannon, C.R., Vellodi, A., Hart, C.A., Sills, J.A.

Journal:

Year:

1984

Language:

english

File:

PDF, 309 KB

english, 1984

98

Limited clinical impact of anti-idursulfase antibodies developed during long-term idursulfase enzyme replacement therapy (ERT) in mucopolysaccharidosis II (MPS II, Hunter syndrome) patients aged 5-35 years

Harmatz, Paul, Giugliani, Roberto, Mendelsohn, Nancy J., Vellodi, Ashok, Kunes, Yune, Sciarappa, Kenneth, Bielefeld, Bonnie, Barbier, Ann J., Pano, Arian, Hendriksz, Christian J., Vijayaraghavan, Sure

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 49 KB

english, 2014

99

Progression of feeding skills in infantile Pompe disease - the GOSH experience

Lozano, Sonia, Vellodi, Ashok, Broomfield, Alexander

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 43 KB

english, 2014

100

Pulmonary disease in type III Gaucher disease refractory to conventional enzyme replacement therapy

Davison, James E., Wallis, Colin, Mauri, Francesco, Berry, Matthew, Vellodi, Ashok

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 138 KB

english, 2014