-
1
-
-
77953157233
-
The clinical presentation of mitochondrial diseases in children with progressive intellectual and neurological deterioration (PIND): a national prospective population-based study
-
Published online September 11th 2009, DOI: 10.1111/j.1469-8749.2009.03463.x
-
Verity C, Winstone AM, Stellitano L, Krishnakumar D. The clinical presentation of mitochondrial diseases in children with progressive intellectual and neurological deterioration (PIND): a national prospective population-based study. Dev Med Child Neurol 10.1111/j.1469-8749.2009.03463.x, Published online September 11th 2009, DOI
-
Dev Med Child Neurol
-
-
Verity, C.1
Winstone, A.M.2
Stellitano, L.3
Krishnakumar, D.4
-
2
-
-
0035092240
-
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA anbormalities
-
Darin N, Oldfors A, Moslemi AR, Holme E, Tulinius M. The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA anbormalities. Ann Neurol 2001, 49:377-83.
-
(2001)
Ann Neurol
, vol.49
, pp. 377-383
-
-
Darin, N.1
Oldfors, A.2
Moslemi, A.R.3
Holme, E.4
Tulinius, M.5
-
3
-
-
14244259670
-
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease
-
Scaglia F, Towbin JA, Craigen WJ. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics 2004, 114:925-31.
-
(2004)
Pediatrics
, vol.114
, pp. 925-931
-
-
Scaglia, F.1
Towbin, J.A.2
Craigen, W.J.3
-
4
-
-
0026583782
-
The neuropsychological features of mitochondrial myopathies and encephalomyopathies
-
Kartsounis LD, Troung DD, Morgan-Hughes JA, Harding AE. The neuropsychological features of mitochondrial myopathies and encephalomyopathies. Arch Neurol 1992, 49:158-60.
-
(1992)
Arch Neurol
, vol.49
, pp. 158-160
-
-
Kartsounis, L.D.1
Troung, D.D.2
Morgan-Hughes, J.A.3
Harding, A.E.4
-
5
-
-
0033957295
-
Neurologic presentations of mitochondrial disorders
-
Nissenkorn A, Zeharia A, Lev D. Neurologic presentations of mitochondrial disorders. J Child Neurol 2000, 15:44-8.
-
(2000)
J Child Neurol
, vol.15
, pp. 44-48
-
-
Nissenkorn, A.1
Zeharia, A.2
Lev, D.3
-
6
-
-
0034058869
-
Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders
-
Uusimaa J, Remes AM, Rantala H. Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders. Pediatrics 2000, 105:598-603.
-
(2000)
Pediatrics
, vol.105
, pp. 598-603
-
-
Uusimaa, J.1
Remes, A.M.2
Rantala, H.3
-
7
-
-
67349192238
-
MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
-
Naess K, Freyer C, Bruhn H. MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. Biochim Biophys Acta 2009, 1789:484-90.
-
(2009)
Biochim Biophys Acta
, vol.1789
, pp. 484-490
-
-
Naess, K.1
Freyer, C.2
Bruhn, H.3
-
8
-
-
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, 21:170-2.
-
(2006)
J Child Neurol
, vol.21
, pp. 170-172
-
-
Poling, J.S.1
Frye, R.E.2
Shoffner, J.3
Zimmerman, A.W.4
-
9
-
-
56849108261
-
Mitochondrial disease in autism spectrum disorder patients: a cohort analysis
-
Weissman JR, Kelley RI, Bauman ML. Mitochondrial disease in autism spectrum disorder patients: a cohort analysis. PLoS ONE 2008, 3:e3815.
-
(2008)
PLoS ONE
, vol.3
-
-
Weissman, J.R.1
Kelley, R.I.2
Bauman, M.L.3
|