Early detection of median nerve compression by Electroneurography can improve outcome in children with Mucopolysaccharidoses by Kim Maincent, Bénédicte Héron, Thierry Billette de Villemeur, Michèle Mayer

Subjects: Get full text

Antibodies to recombinant human alpha-L-iduronidase prevent disease correction in cortical bone in MPS I mice by Sarah C. Hurt, Steven Q. Le, Shih-hsin Kan, Quang D. Bui, Michael D. Brodt, Patricia I. Dickson

Subjects: “…Hurler…”
Get full text

Combining angiotensin receptor blockade and enzyme replacement therapy for vascular disease in mucopolysaccharidosis type I by Sarah C. Hurt, Moin U. Vera, Steven Q. Le, Shih-hsin Kan, Quang Bui, Patricia I. Dickson

Subjects: Get full text

Current Practices for U.S. Newborn Screening of Pompe Disease and MPSI by Elizabeth G. Ames, Rachel Fisher, Mary Kleyn, Ayesha Ahmad

Subjects: Get full text

Orthopedic Pathology in Children with Mucopolysaccharidosis Type I by Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Anait K. Gevorkian, Ludmila M. Kuzenkova, Tatiana V. Podkletnova, Marina A. Babaykina, Anatoly B. Anikin, Galina B. Kuznetsova, Liliya A. Osipova, Konstantin V. Jerdev

Subjects: Get full text

A deletion of IDUA exon 10 in a family of Golden Retriever dogs with an attenuated form of mucopolysaccharidosis type I by Kiterie M. E. Faller, Alison E. Ridyard, Rodrigo Gutierrez‐Quintana, Angie Rupp, Celia Kun‐Rodrigues, Tatiana Orme, Karen L. Tylee, Heather J. Church, Rita Guerreiro, Jose Bras

Subjects: “…Hurler…”
Get full text

Use of neuraxial blockade in cases of anticipated difficult airway in pediatric patients – A safer option by Kapil Kulkarni, Gunjan Singh, Javed Iqbal, Ajit K Singh

Subjects: Get full text

Biomarkers for prediction of skeletal disease progression in mucopolysaccharidosis type I by Troy C. Lund, Terence M. Doherty, Julie B. Eisengart, Rebecca L. Freese, Kyle D. Rudser, Ellen B. Fung, Bradley S. Miller, Klane K. White, Paul J. Orchard, Chester B. Whitley, Lynda E. Polgreen

Subjects: Get full text

Mucopolysaccharridosis type 1 and the challenges in managing this rare genetic disorder in the resource poor setting by A. N. Onyiriuka, Oduwole A. O., Oyenusi E. E., I. O. Oluwayemi, Fakeye-Udeogu O. B., M. Kouyate, C. J. Achonwa, M. Abdullahi

Subjects: “…hurler-scheie syndrome, attenuated mucoplysaccharidosis type 1…”
Get full text

Anesthetic management in children with Hurler′s syndrome undergoing emergency ventriculoperitoneal shunt surgery by Nidhi Gupta, Girija Prasad Rath, Renu Bala, Bapura Kiran Reddy, Arvind Chaturvedi

Subjects: Get full text

Challenging behavior in mucopolysaccharidoses types I–III and day-to-day coping strategies: a cross sectional explorative study by Frederik Hoffmann, Susanne Hoffmann, Kevin Kunzmann, Markus Ries

Subjects: Get full text

Mucopolysaccharidosis Type I by Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Ursula da Silveira Matte, Dafne D. Horovitz, Anneliese Lopes Barth, Guilherme Baldo, Filippo Vairo, Roberto Giugliani

Subjects: Get full text

Rare cases of mucopolysaccharidosis type I in children with Hurler and Hurler-Scheie syndromes by A. E. Babushkin, E. G. Khusnutdinova, E. K. Ryskulova, R. M. Mukhametshina

Subjects: Get full text

Elements of lentiviral vector design toward gene therapy for treating mucopolysaccharidosis I by Li Ou, Michael J. Przybilla, Brenda L. Koniar, Chester B. Whitley

Subjects: Get full text

Long-term follow-up of post hematopoietic stem cell transplantation for Hurler syndrome: Clinical, biochemical, and pathological improvements by Eriko Yasuda, William G. Mackenzie, Kristen D. Ruhnke, Tsutomu Shimada, Robert W. Mason, Jozef Zustin, Paul L. Martin, Mihir M. Thacker, Tadao Orii, Yoshimichi Sai, Shunji Tomatsu

Subjects: “…Hurler syndrome…”
Get full text

A Humoral Immune Response Alters the Distribution of Enzyme Replacement Therapy in Murine Mucopolysaccharidosis Type I by Steven Q. Le, Shih-hsin Kan, Don Clarke, Valentina Sanghez, Martin Egeland, Kristen N. Vondrak, Terence M. Doherty, Moin U. Vera, Michelina Iacovino, Jonathan D. Cooper, Mark S. Sands, Patricia I. Dickson

Subjects: Get full text

An online survey on burden of illness among families with post-stem cell transplant mucopolysaccharidosis type I children in the United States by Therese Conner, Francesca Cook, Vivian Fernandez, Karen Rascati, Vanessa Rangel-Miller

Subjects: Get full text

Successful treatment of corneal hypertrophic scar in Hurler syndrome by Nima Koosha, Matin Irajpour, Zeynab Rostamiyan, Ali Shahsavari, Ali Forouhari, Mohsen Pourazizi

Subjects: Get full text

Rozwój funkcji poznawczych u dzieci z mukopolisacharydozą typu I (choroba Hurler) leczonych enzymatycznie laronidazą by Marta Biernacka, Anna Jakubowska-Winecka, Anna Tylki-Szymańska

Subjects: Get full text

Ameloblastoma in a Three-Year-Old Child with Hurler Syndrome (Mucopolysaccharidosis Type I) by Mattia Di Bartolomeo, Arrigo Pellacani, Sara Negrello, Martina Buchignani, Riccardo Nocini, Gianluca Di Massa, Greta Gianotti, Giuseppe Pollastri, Giacomo Colletti, Luigi Chiarini, Alexandre Anesi

Subjects: Get full text