Literature DB >> 5846830

A new type of idiopathic hyperglycinemia with hypo-oxaluria.

T Gerritsen, E Kaveggia, H A Waisman.   

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Year:  1965        PMID: 5846830

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  12 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Non-ketotic hyperglycinaemia: a new case with late onset.

Authors:  V Leuzzi; S Morano; F Moretti; F Fabbrizi; I Antonozzi
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  The clinical findings in a patient with nonketotic hyperglycinemia.

Authors:  H Reploh; H Gröbe; L Diekmann; D Palm; D B von Bassewitz; W Jenett
Journal:  Z Kinderheilkd       Date:  1973

Review 4.  Oxalic acid metabolism in man: a review.

Authors:  A Hodgkinson; P M Zarembski
Journal:  Calcif Tissue Res       Date:  1968-10-21

5.  Amino acid loading tests in a patient with non-ketotic hyperglycinaemia.

Authors:  T Palmer; V G Oberholzer
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

6.  Non-ketotic hyperglycinaemia in a family with an unusual phenotype.

Authors:  T Ando; W L Nyhan; J Bicknell; R Harris; J Stern
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

7.  Enhanced NMDA conductance can account for epileptiform activity induced by low Mg2+ in the rat hippocampal slice.

Authors:  R D Traub; J G Jefferys; M A Whittington
Journal:  J Physiol       Date:  1994-08-01       Impact factor: 5.182

8.  Iatrogenic and transient hyperglycinemia in patients with phenylketonuria.

Authors:  N Nagata; S Shinozuka; I Matsuda; M Kambe; Y Tsuji
Journal:  Eur J Pediatr       Date:  1979-09       Impact factor: 3.183

Review 9.  The screening of hereditary metabolic defects among newborn infants.

Authors:  D Y Hsia
Journal:  Can Med Assoc J       Date:  1966-08-06       Impact factor: 8.262

10.  Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.

Authors:  F X Coude; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1979-12       Impact factor: 14.808

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