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HYPERGLYCINURIA (disorder)
Known as:
Hyperglycinuria
, GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS
, IMINOGLYCINURIA TYPE II
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An increased concentration of glycine in the urine. [HPO:gcarletti, pmid:18901181, pmid:20240447]
National Institutes of Health
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Related topics
Related topics
4 relations
Broader (2)
Amino Acid Metabolism, Inborn Errors
Urolithiasis
Nonketotic Hyperglycinemia
Propionic acidemia
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Heterozygous mutation in SLC36A2 gene causing hyperglycinuria and nephrolithiasis
MahaAl Harbi
,
F. Mutairi
Journal of Biochemical and Clinical Genetics
2019
Corpus ID: 196657754
Background: Childhood nephrolithiasis cases reported worldwide has been increasing over the last decade. The majority of cases…
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2004
2004
The clinical findings in a patient with nonketotic hyperglycinemia
H. Reploh
,
H. Gröbe
,
L. Diekmann
,
D. Palm
,
D. B. V. Bassewitz
,
W. Jenett
Zeitschrift für Kinderheilkunde
2004
Corpus ID: 23760070
A new case of nonketotic hyperglycinemia is reported. Hyperglycinemia, hyperglycinuria and mental retardation without neutropenia…
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2003
2003
SECONDARY HYPERAMMON & AElig ; MIA : A POSSIBLE MECHANISM FOR VALPROATE ENCEPHALOPATHY
Netherlands K. W. Pondman
2003
Corpus ID: 40167406
Sin,—Hyperglycinsemia, hyperglycinuria,l propionicaciduria2 and Reye’s syndrome3 have been reported in epileptic patients…
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1994
1994
Phenylketonuria with familial hyperglycinuria
J. M. Marques
Journal of Inherited Metabolic Disease
1994
Corpus ID: 31432638
Brockstedt M, Jakobs C, Smit LME et al (1990) A new case of dihydropyrimidine dehydrogenase deficiency. Eur J Pediatr 150: 291…
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1984
1984
[Screening for congenital metabolic diseases in mentally retarded patients in 6 psychiatric institutions of Lower Saxony].
D. Byrd
,
D. Brötling
,
J. Brodehl
,
D. Hunneman
Klinische Pädiatrie
1984
Corpus ID: 23222684
The results of screening for inborn errors of metabolism in patients in six institutions for the mentally retarded in Lower…
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Review
1979
Review
1979
Rare association of hyperglycinuria and lenticonus in two members of the same family.
R. Reccia
,
A. Magli
,
B. Pignalosa
,
N. Sannolo
,
P. Strisciuglio
Ophthalmologica. Journal international d…
1979
Corpus ID: 3356793
2 cases of posterior lenticonus associated with hyperglycinuria without iminoaciduria, found in the same family, were examined…
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1977
1977
[Hyperglycinuria induced by n-dipropylacetate. Possible model of propionic acidemia].
P. Kamoun
,
P. Parvy
,
P. Debray-ritzen
La Nouvelle presse medicale
1977
Corpus ID: 339678
1972
1972
[Study on a case of hyperglycinuria with oxalate calculi and ketoaciduria].
F. Linari
,
R. Ragni
,
P. Stratta
,
R. M. Perolino
Minerva urologica
1972
Corpus ID: 20344445
1967
1967
Hypophosphatemic osteomalacia with hyperglycinuria.
J. Kallmeyer
,
G. Dunea
,
F. D. Schwartz
Annals of Internal Medicine
1967
Corpus ID: 21947431
Excerpt In 1956 Dent and Harris (1) described four patients with hypophosphatemic osteomalacia (phosphate diabetes; vitamin D…
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1962
1962
Acquired vitamin D-resistant osteomalacia: a new variety characterized by hypercalcemia, low serum bicarbonate and hyperglycinuria.
P. Henneman
,
E. Dempsey
,
E. Carroll
,
D. Henneman
Metabolism: Clinical and Experimental
1962
Corpus ID: 40619433