Glucoglycinuria, a new familial syndrome. [J Pediatr. 1962] - PubMed

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[Gluco-glycinuria, a new familial syndrome]. [Helv Paediatr Acta. 1961]
[Gluco-glycinuria, a new familial syndrome].
KAESER H, COTTIER P, ANTENER I. Helv Paediatr Acta. 1961 Dec; 16:586-608.
[Glyco-glycinuric diabetes, a new familial syndrome]. [Bull Schweiz Akad Med Wiss. 1962]
[Glyco-glycinuric diabetes, a new familial syndrome].
KAESER H. Bull Schweiz Akad Med Wiss. 1962 Jan; 17:385-8.
[Associated hereditary diseases]. [Minerva Pediatr. 1961]
[Associated hereditary diseases].
GRANDI F, SACCHI R. Minerva Pediatr. 1961 Sep 29; 13:1305-8.
Review Contemporary management of rhinosinusitis and cystic fibrosis. [Curr Opin Otolaryngol Head Nec...]
Review Contemporary management of rhinosinusitis and cystic fibrosis.
Tandon R, Derkay C. Curr Opin Otolaryngol Head Neck Surg. 2003 Feb; 11(1):41-4.
Review Pseudomonal infection in cystic fibrosis: the battle continues. [Expert Rev Anti Infect Ther. 2...]
Review Pseudomonal infection in cystic fibrosis: the battle continues.
Elkin S, Geddes D. Expert Rev Anti Infect Ther. 2003 Dec; 1(4):609-18.

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. [J Clin Invest. 2008]
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.
Bröer S, Bailey CG, Kowalczuk S, Ng C, Vanslambrouck JM, Rodgers H, Auray-Blais C, Cavanaugh JA, Bröer A, Rasko JE. J Clin Invest. 2008 Dec; 118(12):3881-92. Epub 2008 Nov 6.
HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT. [Arch Dis Child. 1964]
HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.
VISSER HK, VEENSTRA HW, PIK C. Arch Dis Child. 1964 Aug; 39:397-402.
Review INHERITED ENZYME DEFECTS: A REVIEW. [J Clin Pathol. 1963]
Review INHERITED ENZYME DEFECTS: A REVIEW.
HARGREAVES T. J Clin Pathol. 1963 Jul; 16:293-318.

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Glucoglycinuria, a new familial syndrome.
Glucoglycinuria, a new familial syndrome.
J Pediatr. 1962 Sep ;61:386-94.

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