Results 191 to 200 of about 12,201 (238)
Some of the next articles are maybe not open access.
The Indian Journal of Pediatrics, 1999
An 11 year old male presented with headache, vomiting and weakness of right side of body. One day after admission he developed right focal seizures. He had 5 previous episodes of stroke, the first at 11 months age. His milestones were normal upto the first episode but subsequent mile stones were delayed.
S K, Singh +6 more
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An 11 year old male presented with headache, vomiting and weakness of right side of body. One day after admission he developed right focal seizures. He had 5 previous episodes of stroke, the first at 11 months age. His milestones were normal upto the first episode but subsequent mile stones were delayed.
S K, Singh +6 more
openaire +2 more sources
Hypocitrullinemia in patients with MELAS: an insight into the “MELAS paradox”
Journal of the Neurological Sciences, 2005L-citrulline, classified as a nonessential amino acid, is synthesized predominantly via Delta-1-pyrroline carboxylate synthase in the endothelial cells of the small intestine. In mammals, small quantities of citrulline are also produced in nitric oxide synthase-expressing cells. Considering the fact that the enzymes involved in the endogenous synthesis
Ali, Naini +5 more
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Generalized Hamming Weights of Melas Codes and Dual Melas Codes
SIAM Journal on Discrete Mathematics, 1994In this nice and elegant paper the authors determine the second and third generalized Hamming weight of the Melas codes and some results on the second generalized Hamming weight of the dual Melas codes. For this purpose they make use of the theory of elliptic curves over finite fields and the description of the codewords of the dual Melas codes in ...
M Van Der Vlugt
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Journal of Stroke and Cerebrovascular Diseases, 1996
MELAS syndrome is one of several mitochondrial-inherited encephalomyopathies distinguished from the others by its unique stroke-like episodes. A case is presented that illustrates the importance of acknowledging the heteroplasmic nature of this disease when making its diagnosis.
L, Silbert, A, Durocher, J, Biller
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MELAS syndrome is one of several mitochondrial-inherited encephalomyopathies distinguished from the others by its unique stroke-like episodes. A case is presented that illustrates the importance of acknowledging the heteroplasmic nature of this disease when making its diagnosis.
L, Silbert, A, Durocher, J, Biller
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Diagnosis and management of MELAS
Expert Review of Molecular Diagnostics, 2004Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) is the most common maternally inherited mitochondrial disease. An A-->G mutation in the transfer RNA(Leu(UUR)) gene at position 3243 of the mitochondrial DNA accounts for most MELAS cases.
Madhav Thambisetty, Nancy J Newman
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Cryptography and Communications, 2015
zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Adel Alahmadi +5 more
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zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Adel Alahmadi +5 more
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Neuroradiology, 1997
We report two patients with fatal mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Single-photon emission computed tomography (SPECT) with 123I-N-isopropyl-p-iodoamphetamine was more sensitive to the lesions than CT or MRI.
A, Miyamoto +5 more
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We report two patients with fatal mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Single-photon emission computed tomography (SPECT) with 123I-N-isopropyl-p-iodoamphetamine was more sensitive to the lesions than CT or MRI.
A, Miyamoto +5 more
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In the heart of MELAS syndrome
International Journal of Cardiology, 2016no ...
Finsterer, Josef, Zarrouk-Mahjoub, Sinda
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A MELAS phenotype is not necessarily MELAS
Tropical Doctor, 2016Josef, Finsterer, Sinda, Zarrouk-Mahjoub
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