Literature DB >> 4380286

A simple spot screening test for galactosemia.

E Beutler, M C Baluda.   

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Year:  1966        PMID: 4380286

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN: 0022-2143


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  47 in total

1.  Galactosaemia: estimated live birth incidence in New Zealand.

Authors:  I C Lyon; C J Chapman; I B Houston; A M Veale
Journal:  Humangenetik       Date:  1975-05-26

Review 2.  Diagnosis and management of inborn errors of metabolism.

Authors:  J E Wraith
Journal:  Arch Dis Child       Date:  1989-10       Impact factor: 3.791

3.  Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.

Authors:  D M Bradley
Journal:  Arch Dis Child       Date:  1975-04       Impact factor: 3.791

4.  The development and organization of newborn screening programs in Turkey.

Authors:  Başak Tezel; Dilek Dilli; Hilal Bolat; Hatice Sahman; Sema Ozbaş; Deniz Acıcan; Mustafa Ertek; Mehmet Rıfat Köse; Uğur Dilmen
Journal:  J Clin Lab Anal       Date:  2013-12-27       Impact factor: 2.352

5.  Results of newborn screening for galactose metabolic disorders.

Authors:  B Inoue; M Hata; Y Ichiba; H Wada; H Misumi; T Mori
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 6.  Newborn mass screening for galactosemia.

Authors:  S Schweitzer
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183

7.  The Chicago variant of clinical galactosemia.

Authors:  C M Chacko; R S Wappner; I K Brandt; H L Nadler
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

8.  Galactosemia screening with low false-positive recall rate: the Swedish experience.

Authors:  Annika Ohlsson; Claes Guthenberg; Ulrika von Döbeln
Journal:  JIMD Rep       Date:  2011-09-06

9.  Molecular basis for Duarte and Los Angeles variant galactosemia.

Authors:  S D Langley; K Lai; P P Dembure; L N Hjelm; L J Elsas
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

10.  Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.

Authors:  K Tada; H Tateda; S Arashima; K Sakai; T Kitagawa; K Aoki; S Suwa; M Kawamura; T Oura; M Takesada
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

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