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Results of search for 'su:"Mucopolysaccharidosis II"', page 6 of 47
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Authors
Bach, G
Beck, M
Beck, Michael
Bondeson, M L
Bozon, D
Di Natale, P
Froissart, R
Giugliani, Roberto
Harper, P S
Hopwood, J J
Ida, Hiroyuki
Jin, Dong-Kyu
Maire, I
Muenzer, Joseph
Neufeld, E F
Scarpa, Maurizio
Suzuki, Yasuyuki
Tomanin, Rosella
Tylki-Szymańska, Anna
Wraith, J E
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Adolescent
Adult
Child
Child, Preschool
Enzyme Replacement Therapy
Female
Glycosaminoglycans
Humans
Iduronate Sulfatase
Infant
Male
Mucopolysaccharidosis I
Mucopolysaccharidosis II
complications
diagnosis
enzymology
genetics
metabolism
methods
pathology
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101.
Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy) prenatal and neonatal bone lesions and their early postnatal evolution.
[electronic resource]
by
CAFFEY, J
Producer:
20040215
In:
The American journal of roentgenology, radium therapy, and nuclear medicine
vol. 67
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102.
Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy); prenatal and neonatal bone lesions and their early postnatal evolution.
[electronic resource]
by
CAFFEY, J
Producer:
20040215
In:
Bulletin of the Hospital for Joint Diseases
vol. 12
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103.
Gene symbol: IDS. Disease: mucopolysaccharidosis type II (Hunter syndrome).
[electronic resource]
by
Villani, G R D
Pontarelli, G
Kotroni, G
Parenti, G
Sibilio, M
Andria, G
Di Natale, P
Producer:
20061207
In:
Human genetics
vol. 119
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104.
[Mitral echocardiography in hunter syndrome (author's transl)].
[electronic resource]
by
Salazar, J
Ferrández, A
Felipe, J
García, M D
Producer:
19791229
In:
Anales espanoles de pediatria
vol. 12
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105.
Biochemical studies in mucolipidoses II and III.
[electronic resource]
by
Shapiro, L J
Hickman, S
Hall, C W
Neufeld, E F
Producer:
19760301
In:
Birth defects original article series
vol. 11
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106.
[Mucolipidosis type II. Report of 2 suggestive cases].
[electronic resource]
by
Moreira Filho, P F
Nascimento, O J
Cincinatus, D
de Freitas, M R
Producer:
19800426
In:
Arquivos de neuro-psiquiatria
vol. 37
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107.
Ivory-colored papules in a young boy. Mucopolysaccharidosis type II-B (Hunter's syndrome, mild).
[electronic resource]
by
Zivony, D I
Spencer, D M
Qualman, S J
Bechtel, M
Producer:
19950216
In:
Archives of dermatology
vol. 131
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108.
Mucopolysaccharidosis (Hunter's syndrome) in a black family.
[electronic resource]
by
Seedat, Y K
Narrandes, R
Maharaj, I C
Producer:
19810424
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 59
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109.
Ocular histopathology of systemic mucopolysaccharidosis, type II-A (Hunter syndrome, severe).
[electronic resource]
by
McDonnell, J M
Green, W R
Maumenee, I H
Producer:
19860228
In:
Ophthalmology
vol. 92
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110.
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene.
[electronic resource]
by
Hopwood, J J
Bunge, S
Morris, C P
Wilson, P J
Steglich, C
Beck, M
Schwinger, E
Gal, A
Producer:
19940331
In:
Human mutation
vol. 2
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111.
Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review.
[electronic resource]
by
Pinto, Louise L C
Vieira, Taiane A
Giugliani, Roberto
Schwartz, Ida V D
Producer:
20100730
In:
Orphanet journal of rare diseases
vol. 5
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112.
Hunter syndrome and new onset idiopathic thrombocytopenic purpura in a young patient.
[electronic resource]
by
Uz, Burak
Demiroglu, Haluk
Ozcebe, Osman Ilhami
Producer:
20120223
In:
Annals of hematology
vol. 91
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113.
Extensive Mongolian Spots and Lysosomal Storage Diseases.
[electronic resource]
by
Mimouni-Bloch, Aviva
Finezilber, Yael
Rothschild, Michal
Raas-Rothschild, Annick
Producer:
20160802
In:
The Journal of pediatrics
vol. 170
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114.
[Mucopolysaccharidosis in 2 brothers: Hunter's syndrome. Clinical case reports].
[electronic resource]
by
Vitolo, G
Producer:
19750913
In:
Minerva pediatrica
vol. 27
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115.
Psychological status of patients with mucopolysaccharidosis type II and their parents.
[electronic resource]
by
Kuratsubo, Izumi
Suzuki, Yasuyuki
Orii, Koji O
Kato, Tomomi
Orii, Tadao
Kondo, Naomi
Producer:
20090806
In:
Pediatrics international : official journal of the Japan Pediatric Society
vol. 51
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116.
[Early response to idursulfase in a 31-year old male patient with Hunter syndrome].
[electronic resource]
by
Pérez-Calvo, J
Bergua Sanclemente, I
López Moreno, M J
Torralba Cabeza, M Á
Amores Arriaga, B
Producer:
20120105
In:
Revista clinica espanola
vol. 211
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117.
Oral and craniofacial manifestations in a Hunter syndrome patient with hematopoietic stem cell transplantation: A case report.
[electronic resource]
by
Torres, Rafaela de Oliveira
Pintor, Andréa Vaz Braga
Guedes, Fábio Ribeiro
Freitas-Fernandes, Liana Bastos
Barth, Anneliese Lopes
Horovitz, Dafne Dain Gandelman
de Souza, Ivete Pomarico Ribeiro
Producer:
20181221
In:
Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry
vol. 38
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118.
Surgical consideration in Hunter syndrome: a case of hydrocephalus and a case of epidural hematoma.
[electronic resource]
by
Li, Jin
Zhang, Xinyan
Jiang, Tao
Li, Chunde
Producer:
20200730
In:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
vol. 35
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119.
Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes.
[electronic resource]
by
Zlotogora, J
Bach, G
Producer:
19840816
In:
The New England journal of medicine
vol. 311
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120.
Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II.
[electronic resource]
by
Wraith, J Edmond
Producer:
20080923
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 97
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