about
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapyCNS-directed gene therapy for the treatment of neurologic and somatic mucopolysaccharidosis type II (Hunter syndrome)Hunter's polydystrophy (gargoylism) with cardiac lesions and some formes frustesDisc oedema in association with Hunter's syndrome: ocular histopathological findings.Insights into Hunter syndrome from the structure of iduronate-2-sulfataseRecent advances in ophthalmic genetics. Genetic counselling.Mucopolysaccharidoses and mucolipidoses.Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.Gargoylism in a Chinese boy.Mild form of Hunter's syndrome: clinical delineation based on 31 cases.Orthopedic manifestations in patients with mucopolysaccharidosis type II (Hunter syndrome) enrolled in the Hunter Outcome Survey.Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and managementA case of gargoylism.The pathology of the feline model of mucopolysaccharidosis VI.The mucopolysaccharidoses (a review).Gargoylism: A Review of the Principal Features with a Report of Five CasesGargoylism: Report of four cases.Gargoylism in a twin brother and sister.Morquio-Ullrich's Disease: An Inborn Error of Metabolism?Hurler's syndrome. A genetic study in cell culture.Gargoylism: sex-linked transmission in nine malesOrthopaedic aspects of the chondrodystrophies. The dwarf and his orthopaedic problems.Hunter syndrome with late age of presentation: clinical description of a case and review of the literature.Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future.Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.Mucopolysacccharidoses: From understanding to treatment, a century of discoveries.Gargoylism (Chondro-osteo-dystrophy, Hepatosplenomegaly, Deafness) in Two Brothers.Hunter syndrome with its typical heart: a close mimic to rheumatic heartThe clinical features, diagnosis, and osseous lesions of gargoylism exemplified in three siblings.Chondrolipodystrophy; Gargoylism.THE DIAGNOSTIC VALUE OF ISOLATED URINARY MUCOPOLYSACCHARIDES AND OF LYMPHOCYTE INCLUSIONS IN GARGOYLISM.Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic typeA rare case of mucopolysaccharidosis: Hunter syndromePapilloedema in association with Hunter's syndrome.Clinical Presentation of Mucopolysaccharidosis Type II (Hunter's Syndrome).Osteochondrodystrophy (Morquio-Brailsford type); occurrence in three siblings.The oral changes in gargoylism.A case of Hunter syndrome with bilateral retinal detachment.MPS II - Hunter syndromePresentation and Treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome).
P2860
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P2860
description
1917 nî lūn-bûn
@nan
1917 թուականին հրատարակուած գիտական յօդուած
@hyw
1917 թվականին հրատարակված գիտական հոդված
@hy
1917年の論文
@ja
1917年論文
@yue
1917年論文
@zh-hant
1917年論文
@zh-hk
1917年論文
@zh-mo
1917年論文
@zh-tw
1917年论文
@wuu
name
A Rare Disease in Two Brothers
@ast
A Rare Disease in Two Brothers
@en
A Rare Disease in Two Brothers
@nl
type
label
A Rare Disease in Two Brothers
@ast
A Rare Disease in Two Brothers
@en
A Rare Disease in Two Brothers
@nl
prefLabel
A Rare Disease in Two Brothers
@ast
A Rare Disease in Two Brothers
@en
A Rare Disease in Two Brothers
@nl
P1476
A Rare Disease in Two Brothers
@en
P2093
P304
P407
P433
Sect Study Dis Child
P577
1917-01-01T00:00:00Z