Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
about
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneSleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialistHunter Syndrome with Extensive Mongolian Spots.Long-term experience with enzyme replacement therapy (ERT) in MPS II patients with a severe phenotype: an international case series.Cognitive, medical, and neuroimaging characteristics of attenuated mucopolysaccharidosis type II.Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfallsDevelopment of a mnemonic screening tool for identifying subjects with Hunter syndrome.The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of lifeReview of the use of idursulfase in the treatment of mucopolysaccharidosis II.The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensusDevelopment of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future.Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter syndrome)Pituitary function studies in a case of mild Hunter's syndrome (MPS IIB).Anterior Hypopituitarism and Treatment Response in Hunter Syndrome: A Comparison of Two Patients.Successful noninvasive ventilation and enzyme replacement therapy in an adult patient with morbus hunterThree Adult Siblings with Mucopolysaccharidosis Type II (Hunter Syndrome): A Report on Clinical Heterogeneity and 12 Months of Therapy with Idursulfase.A rare case of mucopolysaccharidosis: Hunter syndromeInitial report from the Hunter Outcome Survey.The Hunter syndrome-functional outcomes for clinical understanding scale (HS-FOCUS) questionnaire: evaluation of measurement properties.Idursulfase treatment of Hunter syndrome in children younger than 6 years: results from the Hunter Outcome Survey.Growth pattern and growth prediction of body height in children with mucopolysaccharidosis type II.Growth patterns in children with mucopolysaccharidosis I and II.Airway obstruction and sleep apnea in Hurler and Hunter syndromes.Cognitive and behaviour profiles of children with mucopolysaccharidosis Type II.Workshop Proceedings: Streamlined Development of Safety Assessment Programs Supporting Orphan/Rare Diseases-Are We There Yet?Alterations of mucosa of the larynx and hypopharynx in patients with mucopolysaccharidoses.Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: emphasis on the cardiovascular complication and mortality cases.Ethical considerations in allogeneic hematopoietic cell transplantation for children with slowly fatal conditions.Unrelated umbilical cord blood transplantation in infancy for mucopolysaccharidosis type IIB (Hunter syndrome) complicated by autoimmune hemolytic anemia.Improvement of CNS defects via continuous intrathecal enzyme replacement by osmotic pump in mucopolysaccharidosis type II mice.Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the hunter outcome survey (HOS).Idursulfase: enzyme replacement therapy for mucopolysaccharidosis Type II (Hunter syndrome)Anesthetic Management in Mucopolysaccharidoses
P2860
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P2860
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
description
1982 nî lūn-bûn
@nan
1982 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1982 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
name
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@ast
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@en
type
label
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@ast
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@en
prefLabel
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@ast
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@en
P2860
P356
P1476
Mild form of Hunter's syndrome: clinical delineation based on 31 cases.
@en
P2093
P2860
P304
P356
10.1136/ADC.57.11.828
P407
P577
1982-11-01T00:00:00Z