OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
about
The structure of acid mucopolysaccharides produced by Hurler fibroblasts in tissue culture.The mucopolysaccharidoses.Excretion in the urine of aminoacridine precipitable polyuronides (acid mucopolysaccharides) in patients with rheumatoid arthritis.Phenotypic expression in mucopolysaccharidosis VII.Alpha-L-iduronidase and enzyme replacement therapy for mucopolysaccharidosis I.Study of the Hurler syndrome using cell culture: definition of the biochemical phenotype and the effects of ascorbic acid on the mutant cellIncreased urinary excretion of acidic mucopolysaccharides in exophthalmos.Mucopolysaccharidoses and mucolipidoses.Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.Mucopolysaccharidosis.A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses.HURLER'S SYNDROME: A HISTOCHEMICAL STUDY. NEW TECHNIQUES FOR LOCALIZATION OF VERY WATER-SOLUBLE ACID MUGOPOLYSACCHARIDES.Hepatic ultrastructure in the Hurler syndrome.Acid mucopolysaccharide granules in the glomerular epithelium in gargoylism.Ocular correlates of inborn metabolic defects.The mucopolysaccharidoses (a review).MUCOPOLYSACCHARIDOSIS: PAPER ELECTROPHORETIC AND INFRA-RED ANALYSIS OF THE URINE IN GARGOYLISM AND MORQUIO-ULLRICH'S DISEASE.Hurler's syndrome. A genetic study in cell culture.Hurler's syndrome. Effect of retinol (vitamin A alcohol) on cellular mucopolysaccharides in cultured human skin fibroblasts.Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue cultureLipid abnormalities in a variant of the Hurler syndrome.MRI morphometric characterisation of the paediatric cervical spine and spinal cord in children with MPS IVA (Morquio-Brailsford syndrome).Orthopaedic aspects of the chondrodystrophies. The dwarf and his orthopaedic problems.Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion.TISSUE STORAGE OF MUCOPOLYSACCHARIDES IN HURLER-PFAUNDLER'S DISEASE.Lysosomal storage disease: revealing lysosomal function and physiology.Spinal involvement in mucopolysaccharidoses: a review.Mucopolysacccharidoses: From understanding to treatment, a century of discoveries.The acid mucopolysaccharides. These essential components of living tissue exhibit demonstrable alterations of diagnostic assistance in certain diseases.Detection of inborn errors of metabolism.Urinalysis, critical discipline of clinical science.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 typeHistochemical and electron microscopic study in a case of Hurler's disease.Ultrastructural and biochemical aspects of the Sanfilippo syndrome,--type III genetic mucopolysaccharidosis.A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM.Metaphyseal chondrodysplasia calcificans. A report on two cases.Three siblings with atypical mucopolysaccharidosis.
P2860
Q33562639-A522D3BC-489A-442D-9179-844F2DEE6333Q33586932-23C4A474-1502-4DD1-ABF7-EA4DFB36A666Q33627146-5680BF6F-EB55-4826-B258-B3B273C1FA21Q33628587-930FBD62-D0E2-44BB-ADBA-D66F288F1E1EQ33963579-F1CE6955-6707-4433-8DD4-BA43F4C99C07Q34272120-B3CFEE8E-97DC-4FC1-8114-5F82F6568949Q34280833-41BFE6D9-6DF4-4F60-BDA6-480811AE045FQ34302974-C0C61F81-6221-41D1-92DD-454CEE4476D0Q34540514-7AAB981D-666E-4634-ACA0-32A1C5B1AA73Q35142316-82D9E45F-0EC8-4C32-A7C3-9BEF004B51EBQ35232274-41B5F6AF-7C51-4416-929E-8470FEF6D10AQ35869842-CCB18225-8019-4CA6-99D7-B37284D54482Q35886088-388B4438-4D68-4BDB-A287-28AB90BD51B3Q35916692-E31F902B-C8C9-4E2A-9AB2-5C5B0A48400AQ35920065-2FDC873A-4FA2-488D-BAE2-4C5DD4E0F5B2Q35986296-47CC9DFF-A153-4870-B22F-367CE536EE45Q36060156-35C38F2A-9AA7-4520-B119-3E1CBA2903ADQ36267955-453C585B-5DB2-4336-B8F4-CAA9256C1B29Q36268654-213995D0-1F35-4554-856A-DCF7B8557311Q36384007-B350082B-3864-46D6-AC29-6904D776451EQ36470626-581B54C7-4FA1-468F-8E61-DBE5CEAC73D1Q36662839-860B44A3-A819-4B19-A88E-8528ED5F87A7Q36664188-1D9A524E-5277-42AB-9F22-0F5B88869FD1Q37468016-9190DEE8-2524-4399-96B4-A017FB7AEBB9Q37689876-C2DE1B2A-63DD-487C-8618-4673A372205BQ37739706-EA30AD72-DD8B-4B55-993E-5C9CDA2560D0Q38264031-681781D2-0D3A-40D3-84E8-DC2220294755Q39466972-F9453E61-7E83-4C91-A995-856F7FB12B4EQ39883141-A4B0805A-C370-455F-8E61-78E15595B2DFQ39885597-8911BC75-399A-4B16-AE31-D61921A25CACQ39953457-BF159B77-465C-4A62-BBED-7E2235E27913Q42161737-3677549E-E876-40DD-8A6B-2EF1ADF55CE0Q42165836-790CB535-30C7-4664-BEAA-A29D02C3FBCAQ42414414-E5D3D120-9BCA-41BC-9734-D738C23C535DQ48419336-A1DE7BBC-E6C8-405C-822A-A5D6A6D0556BQ51281682-97634627-1C55-46F9-8047-23408F2BDA5CQ52328530-5C2BCBF0-481E-498E-80CB-69FD874FE046Q54749813-A239D7B2-E1D5-40A5-B640-4F9939434C22
P2860
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 1957
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@en
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@nl
type
label
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@en
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@nl
prefLabel
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@en
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@nl
P2860
P356
P1476
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.
@en
P2093
P2860
P304
P356
10.1073/PNAS.43.6.443
P407
P577
1957-06-01T00:00:00Z