-
2
-
-
0039554477
-
Metabolic diseases of the nervous system
-
Menkes JH, editor. Baltimore: Williams & Wilkins
-
Menkes JH. Metabolic diseases of the nervous system. In: Menkes JH, editor. Textbook of child neurology. Baltimore: Williams & Wilkins; 1995. p. 29-151.
-
(1995)
Textbook of Child Neurology
, pp. 29-151
-
-
Menkes, J.H.1
-
4
-
-
0025886368
-
Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty-nine Japanese patients with urea cycle enzymopathies
-
Nagata N, Matsuda I, Matsura T, Oyanagi K, Tada K, Narisawa K, et al. Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty-nine Japanese patients with urea cycle enzymopathies. Am J Med Genet 1991;40:477-81.
-
(1991)
Am J Med Genet
, vol.40
, pp. 477-481
-
-
Nagata, N.1
Matsuda, I.2
Matsura, T.3
Oyanagi, K.4
Tada, K.5
Narisawa, K.6
-
5
-
-
20044390176
-
Ornithine transcarbamylase deficiency
-
Roth KS, Steiner RD. Ornithine transcarbamylase deficiency. eMedicine 2002;3:2.
-
(2002)
eMedicine
, vol.3
, pp. 2
-
-
Roth, K.S.1
Steiner, R.D.2
-
6
-
-
0028085701
-
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests
-
Spada M, Guardamagna O, Rabier D, van der Meer SB, Parvy P, Bardet J, et al. Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge tests. J Pediatr 1994; 125(2):249-51.
-
(1994)
J Pediatr
, vol.125
, Issue.2
, pp. 249-251
-
-
Spada, M.1
Guardamagna, O.2
Rabier, D.3
Van Der Meer, S.B.4
Parvy, P.5
Bardet, J.6
-
7
-
-
0022642207
-
Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency
-
Batshaw ML, Msall M, Beaudet AL, Trojak J. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency. J Pediatr 1986;108(2):236-41.
-
(1986)
J Pediatr
, vol.108
, Issue.2
, pp. 236-241
-
-
Batshaw, M.L.1
Msall, M.2
Beaudet, A.L.3
Trojak, J.4
-
9
-
-
12944288098
-
Cognitive and behavioural manifestations of metabolic and chromosomal disorders
-
Frank Y, editor. New York: CRC Press
-
Trauner DA. Cognitive and behavioural manifestations of metabolic and chromosomal disorders. In: Frank Y, editor. Pediatric behavioural neurology. New York: CRC Press; 1996. p. 251-68.
-
(1996)
Pediatric Behavioural Neurology
, pp. 251-268
-
-
Trauner, D.A.1
-
10
-
-
0037601722
-
Psychiatric aspects of pediatric disorders
-
Lewis M, editor. Baltimore: Williams & Wilkins
-
Graham PJ, Turk J. Psychiatric aspects of pediatric disorders. In: Lewis M, editor. Child and adolescent psychiatry. Baltimore: Williams & Wilkins; 1996. p. 989-1005.
-
(1996)
Child and Adolescent Psychiatry
, pp. 989-1005
-
-
Graham, P.J.1
Turk, J.2
-
11
-
-
0027351015
-
The neurobiology and genetics of infantile autism
-
Lotspeich LJ, Ciaranello RD. The neurobiology and genetics of infantile autism. Int Rev Neurobiol 1993;35:87-129.
-
(1993)
Int Rev Neurobiol
, vol.35
, pp. 87-129
-
-
Lotspeich, L.J.1
Ciaranello, R.D.2
-
12
-
-
0036244250
-
Biochemical aspects in autism spectrum disorders: Updating the opioid-excess theory and presenting new opportunities for biomedical intervention
-
Whiteley P, Shattock P. Biochemical aspects in autism spectrum disorders: updating the opioid-excess theory and presenting new opportunities for biomedical intervention. Expert Opin Ther Targets 2002;6(2):175-83.
-
(2002)
Expert Opin Ther Targets
, vol.6
, Issue.2
, pp. 175-183
-
-
Whiteley, P.1
Shattock, P.2
-
13
-
-
0032881477
-
Metabolic disorders presenting with behavioral symptoms in the school-aged child
-
Trifiletti RR, Packard AM. Metabolic disorders presenting with behavioral symptoms in the school-aged child. Child Adolesc Psychiatr Clin N Am 1999;8(4):791-806.
-
(1999)
Child Adolesc Psychiatr Clin N Am
, vol.8
, Issue.4
, pp. 791-806
-
-
Trifiletti, R.R.1
Packard, A.M.2
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