-
1
-
-
0034048044
-
Autism associated with the mitochondrial DNA G8363A transfer RNA (Lys) mutation
-
Graf WD, Marin-Garcia J., Gao HG, et al. Autism associated with the mitochondrial DNA G8363A transfer RNA (Lys) mutation. J Child Neurol. 2000;15:357-361.
-
(2000)
J Child Neurol
, vol.15
, pp. 357-361
-
-
Graf, W.D.1
Marin-Garcia, J.2
Gao, H.G.3
-
2
-
-
0036592842
-
Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome
-
Fillano JJ, Goldenthal MJ, Rhodes CH, Marin-Garcia J. Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome. J Child Neurol. 2002;17:435-439.
-
(2002)
J Child Neurol
, vol.17
, pp. 435-439
-
-
Fillano, J.J.1
Goldenthal, M.J.2
Rhodes, C.H.3
Marin-Garcia, J.4
-
3
-
-
9144239818
-
Mitochondrial DNA abnormalities and autistic spectrum disorders
-
Pons R., Andreu AL, Checcarelli N., et al. Mitochondrial DNA abnormalities and autistic spectrum disorders. J Pediatr. 2004;144:81-85.
-
(2004)
J Pediatr
, vol.144
, pp. 81-85
-
-
Pons, R.1
Andreu, A.L.2
Checcarelli, N.3
-
5
-
-
14044258489
-
Mitochondrial dysfunction in autism spectrum disorders: A population-based study
-
Olivera G., Diogo L., Grazina M., et al. Mitochondrial dysfunction in autism spectrum disorders: A population-based study. Dev Med Child Neurol. 2005;47:185-189.
-
(2005)
Dev Med Child Neurol
, vol.47
, pp. 185-189
-
-
Olivera, G.1
Diogo, L.2
Grazina, M.3
-
6
-
-
0004235298
-
-
American Psychiatric Association. 4th ed. Washington, DC: American Psychiatric Association
-
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Washington, DC: American Psychiatric Association; 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
9
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
Lord C., Risi S., Lambrecht L., et al. The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disorder. 2000;30: 205-223.
-
(2000)
J Autism Dev Disorder
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
-
10
-
-
0035836740
-
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency
-
Musumeci O., Naini A., Slonim AE, et al. Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Neurology. 2001;56:849-855.
-
(2001)
Neurology
, vol.56
, pp. 849-855
-
-
Musumeci, O.1
Naini, A.2
Slonim, A.E.3
-
11
-
-
0033837083
-
Practice parameter: Screening and diagnosis of autism: Report of the Quality Standards Subcommittee of the American Academy and the Child Neurology Society
-
Felipek PA, Accardo PJ, Ashwal S., et al. Practice parameter: Screening and diagnosis of autism: Report of the Quality Standards Subcommittee of the American Academy and the Child Neurology Society. Neurology. 2000;55:468-479.
-
(2000)
Neurology
, vol.55
, pp. 468-479
-
-
Felipek, P.A.1
Accardo, P.J.2
Ashwal, S.3
-
12
-
-
0035653670
-
Rosen-Sheiddley B. Genetics of autism: Complex etiology for a heterogeneous disorder
-
Folstein SE, Rosen-Sheiddley B. Genetics of autism: Complex etiology for a heterogeneous disorder. Nature Rev Genet. 2001;2:943-955.
-
(2001)
Nature Rev Genet
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
-
13
-
-
0141427915
-
Epidemiological surveys of autism and other pervasive developmental disorders: An update
-
Fombonne E. Epidemiological surveys of autism and other pervasive developmental disorders: An update. J Autism Dev Disord. 2003;33:365-382.
-
(2003)
J Autism Dev Disord
, vol.33
, pp. 365-382
-
-
Fombonne, E.1
-
15
-
-
0032802683
-
Skeletal muscle mitochondrial defects in nonspecific neurologic disorders
-
Martin-Garcia J., Ananthakrishnan R., Goldenthal MJ, et al. Skeletal muscle mitochondrial defects in nonspecific neurologic disorders. Pediatr Neurol. 1999;21:538-542.
-
(1999)
Pediatr Neurol
, vol.21
, pp. 538-542
-
-
Martin-Garcia, J.1
Ananthakrishnan, R.2
Goldenthal, M.J.3
-
16
-
-
33646830596
-
Developmental regression and mitochondrial dysfunction in a child with autism
-
Poling JS, Frye RE, Shoffner J., Zimmerman AW Developmental regression and mitochondrial dysfunction in a child with autism. J Child Neurol. 2006;21:170-172.
-
(2006)
J Child Neurol
, vol.21
, pp. 170-172
-
-
Poling, J.S.1
Frye, R.E.2
Shoffner, J.3
Zimmerman, A.W.4
-
17
-
-
0027992315
-
Serum serotonin, lactate and pyruvate levels in infantile autistic children
-
Laszlo A., Horvath E., Eck E., Fekete M. Serum serotonin, lactate and pyruvate levels in infantile autistic children. Clin Chim Acta. 1994;229:205-207.
-
(1994)
Clin Chim Acta
, vol.229
, pp. 205-207
-
-
Laszlo, A.1
Horvath, E.2
Eck, E.3
Fekete, M.4
-
18
-
-
0037766224
-
Mitochondrial dysfunction in autistic patients with 15q inverted duplication
-
Filipek AP, Juranek J., Smith M., et al. Mitochondrial dysfunction in autistic patients with 15q inverted duplication. Ann Neurol. 2003;53:801-804.
-
(2003)
Ann Neurol
, vol.53
, pp. 801-804
-
-
Filipek, A.P.1
Juranek, J.2
Smith, M.3
-
19
-
-
0027228506
-
Mitochondrial disorders: Analysis of their clinical and imaging characteristics
-
Barkovich AJ, Good WV, Koch TK, Berg BO Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol. 1993;14:1119-1137.
-
(1993)
AJNR Am J Neuroradiol
, vol.14
, pp. 1119-1137
-
-
Barkovich, A.J.1
Good, W.V.2
Koch, T.K.3
Berg, B.O.4
-
20
-
-
0032471372
-
Neuroradilogic findings in children with mitochondrial disorers
-
Valanne L., Ketonen L., Majander A., et al. Neuroradilogic findings in children with mitochondrial disorers. AJNR Am J Neuroradiol. 1998;369-377.
-
(1998)
AJNR Am J Neuroradiol
, pp. 369-377
-
-
Valanne, L.1
Ketonen, L.2
Majander, A.3
-
21
-
-
27144547046
-
Brain MRI and proton MRS findings in infants and children with respiratory chain defects
-
Dinopoulos A., Cecil KM, Schapiro MB, et al. Brain MRI and proton MRS findings in infants and children with respiratory chain defects. Neuropediatrics. 2005;36:290-301.
-
(2005)
Neuropediatrics
, vol.36
, pp. 290-301
-
-
Dinopoulos, A.1
Cecil, K.M.2
Schapiro, M.B.3
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