Literature DB >> 5086722

Combined vitamin responsiveness in homocystinuria.

G Morrow, L A Barness.   

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Year:  1972        PMID: 5086722     DOI: 10.1016/s0022-3476(72)80548-1

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


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  7 in total

1.  Homocystinuria.

Authors:  D M Isherwood
Journal:  BMJ       Date:  1996-10-26

2.  Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion.

Authors:  J R Poole; S H Mudd; E B Conerly; W A Edwards
Journal:  J Clin Invest       Date:  1975-05       Impact factor: 14.808

3.  Homocystinuria in New South Wales.

Authors:  B Wilcken; G Turner
Journal:  Arch Dis Child       Date:  1978-03       Impact factor: 3.791

4.  The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

Authors:  S H Mudd; F Skovby; H L Levy; K D Pettigrew; B Wilcken; R E Pyeritz; G Andria; G H Boers; I L Bromberg; R Cerone
Journal:  Am J Hum Genet       Date:  1985-01       Impact factor: 11.025

5.  Inborn errors of metabolism. Vitamin-responsive genetic disease.

Authors:  S H Mudd
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

6.  Homocystinuria: A rare condition presenting as stroke and megaloblastic anemia.

Authors:  Parveen Bhardwaj; Ravi Sharma; Minoo Sharma
Journal:  J Pediatr Neurosci       Date:  2010-07

Review 7.  Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Authors:  Andrew A M Morris; Viktor Kožich; Saikat Santra; Generoso Andria; Tawfeg I M Ben-Omran; Anupam B Chakrapani; Ellen Crushell; Mick J Henderson; Michel Hochuli; Martina Huemer; Miriam C H Janssen; Francois Maillot; Philip D Mayne; Jenny McNulty; Tara M Morrison; Helene Ogier; Siobhan O'Sullivan; Markéta Pavlíková; Isabel Tavares de Almeida; Allyson Terry; Sufin Yap; Henk J Blom; Kimberly A Chapman
Journal:  J Inherit Metab Dis       Date:  2016-10-24       Impact factor: 4.982

  7 in total

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