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Results of search for 'su:"Mucopolysaccharidoses"', page 45 of 109
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Authors
Cantz, M
Constantopoulos, G
Danes, B S
Desnick, R J
Dorfman, A
Giugliani, Roberto
Haskins, M E
Hopwood, J J
Jezyk, P F
Krasnopol'skaia, K D
Kresse, H
Lin, Shuan-Pei
Matalon, R
Neufeld, E F
Ockerman, P A
Orii, T
Patterson, D F
Spranger, J
Tomatsu, Shunji
von Figura, K
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Adolescent
Adult
Child
Child, Preschool
Female
Fibroblasts
Glycosaminoglycans
Humans
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Mucopolysaccharidoses
analysis
complications
diagnosis
enzymology
etiology
genetics
metabolism
pathology
urine
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Results
881.
An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum.
[electronic resource]
by
Brooks, Doug A
Gibson, Gary J
Karageorgos, Litsa
Hein, Leanne K
Robertson, Evelyn F
Hopwood, John J
Producer:
20050914
In:
Molecular genetics and metabolism
vol. 85
Online resources:
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882.
Magnetic resonance imaging findings in Hunter syndrome.
[electronic resource]
by
Finn, Chelsea T
Vedolin, Leonardo
Schwartz, Ida V
Giugliani, Roberto
Haws, Charlotte A
Prescot, Andrew P
Renshaw, Perry F
Producer:
20080923
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 97
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883.
Accumulation of 32S-mucopolysaccharides in cultured mucolipidosis cells.
[electronic resource]
by
Hieber, V
Distler, J
Jourdian, G W
Schmickel, R
Producer:
19760301
In:
Birth defects original article series
vol. 11
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884.
Comprehensive urinary screening for inborn errors of complex carbohydrate metabolism.
[electronic resource]
by
Sewell, A C
Gehler, J
Spranger, J
Producer:
19790917
In:
Klinische Wochenschrift
vol. 57
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885.
Mucopolysaccharidosis and lipidosis in rats treated with tilorone analogues.
[electronic resource]
by
Hein, L
Lüllmann-Rauch, R
Producer:
19891109
In:
Toxicology
vol. 58
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886.
[Value of cerebral biopsy in children with chronic cerebral diseases].
[electronic resource]
by
Vigouroux, R P
Toga, M
Choux, M
Baurand, C
Dubois, D
Perrimond, H
Producer:
19680121
In:
Neuro-Chirurgie
vol. 13
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887.
Arylsulfatase B activity in cultured retinal pigment epithelium: regional studies in feline mucopolysaccharidosis VI.
[electronic resource]
by
Stramm, L E
Desnick, R J
Haskins, M E
Aguirre, G D
Producer:
19860808
In:
Investigative ophthalmology & visual science
vol. 27
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888.
Incidence of genetic factors in the causation of deafness in childhood.
[electronic resource]
by
Lenzi, A
Zaghis, A
Producer:
19890328
In:
Scandinavian audiology. Supplementum
vol. 30
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889.
The clinical spectrum of alpha-L-iduronidase deficiency.
[electronic resource]
by
Roubicek, M
Gehler, J
Spranger, J
Producer:
19850528
In:
American journal of medical genetics
vol. 20
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890.
Isolation and characterization of N-acetylglucosamine 6-sulfate from the urine of a patient with Sanfilippo type D syndrome and its occurrence in normal urine.
[electronic resource]
by
Hopwood, J J
Elliott, H
Producer:
19841102
In:
Biochemistry international
vol. 6
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891.
Hybridization studies of fibroblasts from Hurler, Scheie, and Hurler/Scheie compound patients: support for the hypothesis of allelic mutants.
[electronic resource]
by
Fortuin, J J
Kleijer, W J
Producer:
19800514
In:
Human genetics
vol. 53
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892.
[Hereditary chondrodysplasias].
[electronic resource]
by
Piffaretti, P G
Producer:
19690919
In:
Radiologia clinica et biologica
vol. 38
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893.
[Mucopolysaccharidoses in clinical practice].
[electronic resource]
by
Szabó, L
Producer:
19720711
In:
Orvosi hetilap
vol. 113
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894.
[Radiographic changes in mucopolysaccharidoses].
[electronic resource]
by
Kozlowski, K
Zychowicz, C
Producer:
19700205
In:
Polski przeglad radiologii i medycyny nuklearnej
vol. 33
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895.
Determination of heterozygous carrier state from the urine of the parents of children suffering from mucopolysaccharidosis.
[electronic resource]
by
Józsa, L
Szabó, L
Producer:
19730412
In:
Acta paediatrica Academiae Scientiarum Hungaricae
vol. 13
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896.
Decrease of urinary acid mucopolysaccharides in Hurler's syndrome after plasma infusion.
[electronic resource]
by
Orii, T
Yamaguchi, M
Minami, R
Nakao, T
Producer:
19741116
In:
The Tohoku journal of experimental medicine
vol. 112
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897.
[The heparitinsulfate mucopolysaccharidosis (Sanfilippo). Clinical, biochemical, genetic and morphological studies].
[electronic resource]
by
Teller, W
Bechtelsheimer, H
Totović, V
Producer:
19680630
In:
Klinische Wochenschrift
vol. 45
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898.
Urinary glycosaminoglycans and the direct quantification of irregular spots on thin-layer chromatograms.
[electronic resource]
by
Samuels, S
Fisher, C
Micca, P S
Veliz, G
Producer:
19740821
In:
Journal of chromatography
vol. 92
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899.
Hand disorders in children with mucopolysaccharide storage diseases.
[electronic resource]
by
Holt, Joshua B
Van Heest, Ann E
Shah, Apurva S
Producer:
20140717
In:
The Journal of hand surgery
vol. 38
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900.
Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patient.
[electronic resource]
by
Gordon, B A
Feleki, V
Budreau, C H
Tyler, L
Producer:
19751021
In:
Clinical biochemistry
vol. 8
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