-
1
-
-
84864102232
-
GLUT1 deficiency syndrome in clinical practice
-
J. Klepper GLUT1 deficiency syndrome in clinical practice Epilepsy Res. 100 2012 272 277
-
(2012)
Epilepsy Res.
, vol.100
, pp. 272-277
-
-
Klepper, J.1
-
2
-
-
84866054022
-
Glucose transporter type i deficiency syndrome: Epilepsy phenotypes and outcomes
-
A.W. Pong, B.R. Geary, K.M. Engelstad, A. Natarajan, H. Yang, and D.C. De Vivo Glucose transporter type I deficiency syndrome: epilepsy phenotypes and outcomes Epilepsia. 53 2012 1503 1510
-
(2012)
Epilepsia.
, vol.53
, pp. 1503-1510
-
-
Pong, A.W.1
Geary, B.R.2
Engelstad, K.M.3
Natarajan, A.4
Yang, H.5
De Vivo, D.C.6
-
3
-
-
0036791941
-
Imaging the metabolic footprint of Glut1 deficiency on the brain
-
J.M. Pascual, R.L. Van Heertum, D. Wang, K. Engelstad, and D.C. De Vivo Imaging the metabolic footprint of Glut1 deficiency on the brain Ann Neurol. 52 2002 458 464
-
(2002)
Ann Neurol.
, vol.52
, pp. 458-464
-
-
Pascual, J.M.1
Van Heertum, R.L.2
Wang, D.3
Engelstad, K.4
De Vivo, D.C.5
-
4
-
-
0037162369
-
Distinctly abnormal brain metabolism in late-onset ornithine transcarbamylase deficiency
-
J. Takanashi, A. Kurihara, and M. Tomita Distinctly abnormal brain metabolism in late-onset ornithine transcarbamylase deficiency Neurology. 59 2002 210 214
-
(2002)
Neurology.
, vol.59
, pp. 210-214
-
-
Takanashi, J.1
Kurihara, A.2
Tomita, M.3
-
5
-
-
0032706872
-
Inflammatory CNS demyelination: Histopathologic correlation with in vivo quantitative proton MR spectroscopy
-
A. Bitsch, H. Bruhn, and V. Vougioukas Inflammatory CNS demyelination: histopathologic correlation with in vivo quantitative proton MR spectroscopy AJNR Am J Neuroradiol 20 1999 1619 1627
-
(1999)
AJNR Am J Neuroradiol
, vol.20
, pp. 1619-1627
-
-
Bitsch, A.1
Bruhn, H.2
Vougioukas, V.3
-
6
-
-
34547536885
-
GLUT1 deficiency with delayed myelination responding to ketogenic diet
-
J. Klepper, V. Engelbrecht, H. Scheffer, M.S. van der Knaap, and A. Fiedler GLUT1 deficiency with delayed myelination responding to ketogenic diet Pediatr Neurol. 37 2007 130 133
-
(2007)
Pediatr Neurol.
, vol.37
, pp. 130-133
-
-
Klepper, J.1
Engelbrecht, V.2
Scheffer, H.3
Van Der Knaap, M.S.4
Fiedler, A.5
-
7
-
-
33645736830
-
Longitudinal MRI findings of glucose transporter i deficiency syndrome (Glut-1DS) in a Japanese patient - Longitudinal investigation of multifocal T2 prolonged subcortical lesions, Case Report
-
[in Japanese]
-
N. Kamio, K. Imai, and K. Yanagihara Longitudinal MRI findings of glucose transporter I deficiency syndrome (Glut-1DS) in a Japanese patient - longitudinal investigation of multifocal T2 prolonged subcortical lesions, Case Report [in Japanese] No To Hattatsu (Tokyo) 38 2006 54 56
-
(2006)
No to Hattatsu (Tokyo)
, vol.38
, pp. 54-56
-
-
Kamio, N.1
Imai, K.2
Yanagihara, K.3
-
8
-
-
34547512160
-
GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins [abstract]
-
M. Henneke, D. Wang, and R. Korinthenberg GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins [abstract] Neuropediatrics. 36 2005 140
-
(2005)
Neuropediatrics.
, vol.36
, pp. 140
-
-
Henneke, M.1
Wang, D.2
Korinthenberg, R.3
-
9
-
-
0030975319
-
Specific changes in human brain after hypoglycemic injury
-
M. Fujioka, K. Okuchi, K.I. Hiramatsu, T. Sakaki, S. Sakaguchi, and Y. Ishii Specific changes in human brain after hypoglycemic injury Stroke. 28 1997 584 587
-
(1997)
Stroke.
, vol.28
, pp. 584-587
-
-
Fujioka, M.1
Okuchi, K.2
Hiramatsu, K.I.3
Sakaki, T.4
Sakaguchi, S.5
Ishii, Y.6
-
10
-
-
2342550655
-
Brain damage in glycogen storage disease type i
-
D. Melis, G. Parenti, and R. Della Casa Brain damage in glycogen storage disease type I J Pediatr. 144 2004 637 642
-
(2004)
J Pediatr.
, vol.144
, pp. 637-642
-
-
Melis, D.1
Parenti, G.2
Della Casa, R.3
-
11
-
-
0034775754
-
Reversible brain atrophy and subcortical high signal on MRI in a patient with anorexia nervosa
-
A. Drevelengas, D. Chourmouzi, G. Pitsavas, A. Charitandi, and G. Boulogianni Reversible brain atrophy and subcortical high signal on MRI in a patient with anorexia nervosa Neuroradiology. 43 2001 838 840
-
(2001)
Neuroradiology.
, vol.43
, pp. 838-840
-
-
Drevelengas, A.1
Chourmouzi, D.2
Pitsavas, G.3
Charitandi, A.4
Boulogianni, G.5
-
12
-
-
34447109475
-
3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment
-
D.I. Zafeiriou, E. Vargiami, E. Mayapetek, P. Augoustidou-Savvopoulou, and G.A. Mitchell 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment Pediatr Neurol. 37 2007 47 50
-
(2007)
Pediatr Neurol.
, vol.37
, pp. 47-50
-
-
Zafeiriou, D.I.1
Vargiami, E.2
Mayapetek, E.3
Augoustidou-Savvopoulou, P.4
Mitchell, G.A.5
|