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Results of search for 'su:"Mucopolysaccharidoses"', page 81 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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Topics
Adolescent
Adult
Child
Child, Preschool
Female
Fibroblasts
Glycosaminoglycans
Humans
Infant
Male
Mucopolysaccharidoses
analysis
complications
diagnosis
enzymology
etiology
genetics
metabolism
pathology
urine
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Results
1601.
Anaesthesia and mucopolysaccharidoses. A review of airway problems in children.
[electronic resource]
by
Walker, R W
Darowski, M
Morris, P
Wraith, J E
Producer:
19950320
In:
Anaesthesia
vol. 49
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1602.
Measuring corneal clouding in patients suffering from mucopolysaccharidosis with the Pentacam densitometry programme.
[electronic resource]
by
Elflein, H M
Hofherr, T
Berisha-Ramadani, F
Weyer, V
Lampe, C
Beck, M
Pitz, S
Producer:
20130823
In:
The British journal of ophthalmology
vol. 97
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1603.
Thoracolumbar kyphosis in patients with mucopolysaccharidoses: clinical outcomes and predictive radiographic factors for progression of deformity.
[electronic resource]
by
Roberts, S B
Dryden, R
Tsirikos, A I
Producer:
20160620
In:
The bone & joint journal
vol. 98-B
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1604.
Oral health status in patients with mucopolysaccharidoses.
[electronic resource]
by
Ballıkaya, Elif
Eymirli, Pınar Serdar
Yıldız, Yılmaz
Avcu, Nihal
Sivri, Hatice Serap
Uzamış-Tekçiçek, Meryem
Producer:
20190506
In:
The Turkish journal of pediatrics
vol. 60
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1605.
Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
[electronic resource]
by
Toledo, S P
Saldanha, P H
Lamego, C
Mourão, P A
Dietrich, C P
Mattar, E
Producer:
19800228
In:
American journal of medical genetics
vol. 4
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1606.
[Type 2 mucolipidosis, or inclusion cell disease. Apropos of 3 cases with corneal lesions].
[electronic resource]
by
Blanck, M F
Producer:
19740612
In:
Bulletin des societes d'ophtalmologie de France
vol. 73
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1607.
[2 further cases of Dyggve-Melchior-Clausen syndrome with hypoplasia of the odontoid apophysis and spinal compression].
[electronic resource]
by
Naffah, J
Taleb, N
Producer:
19751010
In:
Archives francaises de pediatrie
vol. 31
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1608.
[The eye and congenital metabolic disorders of the connective tissue].
[electronic resource]
by
Wollensak, J
Producer:
19700109
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 154
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1609.
The spinal disorders in diastrophic dwarfism.
[electronic resource]
by
Herring, J A
Producer:
19780628
In:
The Journal of bone and joint surgery. American volume
vol. 60
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1610.
Widespread abnormalities of radiocolloid distribution in patients with mycopolysaccharidoses.
[electronic resource]
by
Klingensmith, W C
Eikman, E A
Maumenee, I
Wanger, H N
Producer:
19760126
In:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
vol. 16
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1611.
Chemical diagnosis of inborn lysosomal storage disorders involving the eye.
[electronic resource]
by
Dawson, G
Tsay, G C
Producer:
19761029
In:
Birth defects original article series
vol. 12
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1612.
[Metabolic disorders of glycoproteins in congenital glycosidase deficiencies].
[electronic resource]
by
Yamashita, K
Producer:
19841019
In:
Seikagaku. The Journal of Japanese Biochemical Society
vol. 56
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1613.
Beta-glucuronidase deficiency mucopolysaccharidosis.
[electronic resource]
by
Sly, W S
Brot, F E
Glaser, J
Stahl, P D
Quinton, B A
Rimoin, D L
McAlister, W H
Producer:
19750829
In:
Birth defects original article series
vol. 10
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1614.
[Diagnosis of hereditary mucopolysaccharidoses].
[electronic resource]
by
Onisawa, J
Ri, N
Nakamura, R
Mizuno, T
Suzuki, Y
Producer:
19730405
In:
Nihon Hifuka Gakkai zasshi. The Japanese journal of dermatology
vol. 82
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1615.
[Metabolic anomaly involving acid mucopolysaccharides-with reference to the current progress in biochemistry].
[electronic resource]
by
Usui, T
Producer:
19690725
In:
Nihon rinsho. Japanese journal of clinical medicine
vol. 27
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1616.
Beta-glucuronidase deficiency (mucopolysaccharidosis type VII).
[electronic resource]
by
Beaudet, A L
Ferrante, N M
Ferry, G D
Nichols, B L
Producer:
19750829
In:
Birth defects original article series
vol. 10
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1617.
[Mucosulfatidosis. Study of 3 familial cases].
[electronic resource]
by
Couchot, J
Pluot, M
Schmauch, M A
Pennaforte, F
Fandre, M
Producer:
19750826
In:
Archives francaises de pediatrie
vol. 31
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1618.
Gas-liquid chromatographic measurement of glucosamine and galactosamine content of urinary glycosaminoglycans.
[electronic resource]
by
Murphy, D
Pennock, C A
London, K J
Producer:
19740917
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 53
Online resources:
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1619.
[Clinical, radiological, biochemical, and genetic aspects of the Sanfilippo disease, apropos of 3 cases].
[electronic resource]
by
Dhondt, J L
Farriaux, J P
Fournier, A
Fontaine, G
Producer:
19750110
In:
Journal de genetique humaine
vol. 22
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1620.
Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses.
[electronic resource]
by
Lin, Hsiang-Yu
Shih, Shou-Chuan
Chuang, Chih-Kuang
Chen, Ming-Ren
Niu, Dau-Ming
Lin, Shuan-Pei
Producer:
20140102
In:
Orphanet journal of rare diseases
vol. 8
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