Literature DB >> 402458

Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome.

I Liebaers, P Di Natale, E F Neufeld.   

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Year:  1977        PMID： 402458     DOI： 10.1016/s0022-3476(77)80707-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  13 in total

1.  Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes.

Authors:  T Yutaka; A L Fluharty; R L Stevens; H Kihara
Journal:  Am J Hum Genet       Date:  1978-11       Impact factor: 11.025

2.  Hunter syndrome: prenatal diagnosis in maternal serum.

Authors:  J Zlotogora; G Bach
Journal:  Am J Hum Genet       Date:  1986-02       Impact factor: 11.025

3.  Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency disorder fibroblasts.

Authors:  A L Fluharty; R L Stevens; L L Davis; L J Shapiro; H Kihara
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

4.  Biochemical diagnosis of mucopolysaccharidoses: experience of 297 diagnoses in a 15-year period (1977-1991).

Authors:  P Di Natale; T Annella; A Daniele; T De Luca; E Morabito; R Pallini; P Rosario; G Spagnuolo
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

5.  X-linked Hunter syndrome: the heterozygous phenotype in cell culture.

Authors:  B R Migeon; J A Sprenkle; I Liebaers; J F Scott; E F Neufeld
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

6.  Prenatal detection of inherited disorders.

Authors:  C Dwivedi
Journal:  J Natl Med Assoc       Date:  1981-03       Impact factor: 1.798

7.  Detection of hunter heterozygotes by enzymatic analysis of hair roots.

Authors:  N Nwokoro; E F Neufeld
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

8.  The iduronate sulphatase activities of cells and tissue fluids from patients with Hunter syndrome and normal controls.

Authors:  M F Dean
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

9.  The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?

Authors:  E F Neufeld; I Liebaers; C J Epstein; S Yatziv; A Milunsky; B R Migeon
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

10.  Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome.

Authors:  T Tønnesen; F Güttler; C Lykkelund
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
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