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• Airway management in Hurler's syndrome: A persistent challenge for anaesthesiologists

  Authors:Sukhyanti Kerai, Vandana Saith, Rakesh Kumar, and Saipriya TewariFrom:Indian Journal of Anaesthesia (Vol. 60, Issue 8) Peer-Reviewed

  Aug. 20161,393 words Clinical report 1470LByline: Sukhyanti. Kerai, Vandana. Saith, Rakesh. Kumar, Saipriya. Tewari INTRODUCTION The difficulty in airway management of Hurler's syndrome or mucopolysaccharidosis (MPS) type I patients has been described as...

• Hurler syndrome with a tuft of hair

  Authors:Binodini Behera, D. Jena, R. Chhetia, and J. VijayashreeFrom:Indian Journal of Dermatology, Venereology, and Leprology (Vol. 72, Issue 2) Peer-Reviewed

  March-April 20061,096 words Disease/Disorder ove... 1640LByline: Binodini. Behera, D. Jena, R. Chhetia, J. Vijayashree A 2-year-old girl presented with coarse, thick hairy skin all over the body, a tuft of hair in the parietal region, coarse facial features and a prominent...

• Gross motor development of children with Hurler syndrome after umbilical cord blood transplantation

  Authors:Stacey C. Dusing, Deborah E. Thorpe, Michele D. Poe, Angela E. Rosenberg, Vicki S. Mercer, and Maria L. EscolarFrom:Physical Therapy (Vol. 87, Issue 11) Peer-Reviewed

  Nov. 20074,421 words Clinical report 1680LBackground and Purpose Little is known about the gross motor development of children with Hurler syndrome who have undergone umbilical cord blood transplantation (UCBT). The purpose of this study was to provide a...

• Encapsulated engineered myoblasts can cure Hurler syndrome: preclinical experiments in the mouse model

  Authors:E. Piller Puicher, R. Tomanin, M. Salvalaio, A. Friso, G. Hortelano, O. Marin, et al.From:Gene Therapy (Vol. 19, Issue 4) Peer-Reviewed

  Apr. 20126,637 words Report 1590LMucopolysaccharidosis type I (MPSI) is an autosomic recessive, lysosomal storage disorder due to the deficit of the enzyme [alpha]-L-iduronidase (IDUA). The disease accounts for a general impairment of tissue and organ...

• Anesthetic management in children with Hurler's syndrome undergoing emergency ventriculoperitoneal shunt surgery

  Authors:Nidhi Gupta, Girija Rath, Renu Bala, Bapura Reddy, and Arvind ChaturvediFrom:Saudi Journal of Anaesthesia (Vol. 6, Issue 2) Peer-Reviewed

  April-June 20121,761 words Article 1490LByline: Nidhi. Gupta, Girija. Rath, Renu. Bala, Bapura. Reddy, Arvind. Chaturvedi Mucopolysaccharidoses (MPSs) are a group of lysosomal storage disorder characterized by progressive multiorgan accumulation of...

• Laronidase

  From:Formulary (Vol. 38, Issue 6) Peer-Reviewed

  June 200319 words Brief article Laronidase (Aldurazyme, Genzyme/BioMarin) is the first treatment approved for the Hurler and Hurler-Scheie forms of mucopolysaccharidosis I (MPS I)....

• MultiStem

  From:Formulary (Vol. 47, Issue 8) Peer-Reviewed

  Aug. 201220 words Brief article 1350L* Proprietary cell therapy (MultiStem, Athersys) for the treatment of Hurler's syndrome, also known as mucopolysaccharidosis type I or MPS-I....

• Obstructed umbilical hernia in a child with Hurler's syndrome

  Authors:Goutham Gopinath, P. Nagaraj, and M. KulkarniFrom:Indian Journal of Surgery (Vol. 67, Issue 1) Peer-Reviewed

  January-February 20051,176 words Article Byline: Goutham. Gopinath, P. Nagaraj, M. Kulkarni Hurler's syndrome (MPS I-H) is a lysosomal storage disorder characterized by physical deformities and developmental anomalies and premature death. Deficiency of the...

• Temporal and spatial gait characteristics of children with Hurler syndrome after umbilical cord blood transplantation

  Authors:Stacey C. Dusing, Deborah E. Thorpe, Vicki S. Mercer, Angela E. Rosenberg, Michele D. Poe, and Maria L. EscolarFrom:Physical Therapy (Vol. 87, Issue 8) Peer-Reviewed

  Aug. 20073,960 words Article 1720LBackground and Purpose Recent medical advances are increasing the life expectancy of children with Hurler syndrome; however, little is known about the motor abilities of children who have received these medical...