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Bibliografía
[1.]
T. Gerritsen, E. Kaveggia, H.A. Waisman.
A new type of idiopathic hyperglycinemia with hypo-oxaluria..
Pediatrics, 36 (1965), pp. 882
[2.]
K. Hayasaka, K. Tada, N. Fueki.
Nonketotic hyperglycinemia:Analysis of glycine cleavage system in typical and atypical cases..
J Pediatr, 110 (1987), pp. 873-877
[3.]
H. Koyata, K. Hiraga.
The glycine celavage system: Structure of a cDNA encoding human H-protein, and partial characterization of its gene in patients with hyperglycinemias..
Am J Hum Genet, 48 (1991), pp. 351-361
[4.]
K. Tada.
Nonketotic hyperglycinemia. Clinical and metabolic aspects..
Enzyme, 38 (1987), pp. 27-35
[5.]
A. Hamosh, J.V. Hohnston, D. Valle.
McGraw-Hill, (1997),
[6.]
F.I. Lu, P.J. Wang, W.I. Hwu, K.L. Tou Yav, T.R. Wang.
Neonatal type of nonketotic hyperglycinemia..
Pediatr Neurol, 20 (1999), pp. 295-300
[7.]
Y. Ohya, N. Ochi, N. Lizotani, C. Hayakawa, K. Watanabe.
Nonketotic hyperglycinemia: Treatment with NMDA antagonist and conconsideration of neuropathogenesis..
Pediatr Neurol, 7 (1990), pp. 65-68
[8.]
A. Hamosh, J. McDonald, D. Valle, C. Francomano, E. Niedermeyer, M. Johnston.
Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infant..
J Pediatr, 121 (1992), pp. 131-135
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