Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Marilena Alexianu"'
Publikováno v:
Romanian Journal of Neurology, Vol 9, Iss 4, Pp 175-180 (2010)
Mitochondrial diseases can present at any age and include a combination of multisystemic symptoms. Major manifestations of muscle involvement include infantile hypotonia, weakness, and lactic acidosis; severe exercise intolerance and easy fatigabilit
Externí odkaz:
https://doaj.org/article/cd31d0dac3a6437eaa43550c1a9ca1b1
Autor:
Marilena Alexianu, Andrei Dan
Publikováno v:
Romanian Journal of Neurology, Vol 8, Iss 4, Pp 178-184 (2009)
Amyloidosis is the name given to a group of diseases characterized by the extracellular deposition of insoluble amyloid fibrils in different tissues and organs like kidneys, heart, liver, skin, nerves etc. Clinical manifestations of amyloidosis are d
Externí odkaz:
https://doaj.org/article/de038fd881a9468ba296e056a7c76199
Publikováno v:
Romanian Journal of Neurology, Vol 7, Iss 2, Pp 79-82 (2008)
We present a male patient aged 46 years, with gait difficulties and predominant proximal weakness in the lower limbs with insidious onset and slowly progression. EMG indicated an active chronic myopathy, NCV and serum CK levels were in normal limits.
Publikováno v:
Romanian Journal of Neurology, Vol 5, Iss 1, Pp 7-10 (2006)
Distrofia musculară facio-scapulo-humerală (DFSH) este unul dintre cele mai frecvente tipuri de distrofii musculare. În ultimii ani, la tabloul clinic clasic al bolii (caracterizat prin afectarea musculaturii faciale, scapulohumerale, tibiale ante
Publikováno v:
Romanian Journal of Neurology, Vol 4, Iss 3, Pp 126-129 (2005)
Bolnavii cu distrofinopatii pot actualmente beneficia de un diagnostic de acuratețe (incluzând chiar identificarea defectului genetic cauzator), dar nu și de un tratament eficace în a preveni invaliditatea și decesul. Articolul trece în revist
Publikováno v:
Romanian Journal of Neurology, Vol 4, Iss 3, Pp 122-125 (2005)
Distrofinopatiile (distrofia musculară Duchenne, distrofia musculară Becker, cardiomiopatia dilatativă legată de cromozomul X) sunt miopatiidatorate unor mutații ale genei care codează proteina sarcolemală denumită distrofină. Diagnosticul,
Autor:
Voichita Mogos, Marilena Alexianu, Aurora Constantinescu, Adina Manolachie, Alina Daniela Fadur, Ioana Vasiliu, Letitia Leustean, Carmen Vulpoi, Jeanina Idriniceanu, Ioana Bodescu
Publikováno v:
Endocrine Abstracts.
Autor:
Inimioara Mihaela, Cojocaru, Marilena, Alexianu, Alexandra, Bastian, Violeta, Sapira, Cristina, Herţea, M, Cojocaru
Publikováno v:
Romanian journal of internal medicine = Revue roumaine de medecine interne. 50(4)
The authors present the case of a 65-year-old woman who was admitted for paraparesis and paresthesias in the inferior limbs. The neurological examination revealed the difficulty in extension of the right foot and of the right toe, accompanied by pare
Autor:
Inimioara Mihaela, Cojocaru, Gabriela, Socoliuc, Violeta, Sapira, Alexandra, Bastian, Marilena, Alexianu, M, Moldovan
Publikováno v:
Romanian journal of internal medicine = Revue roumaine de medecine interne. 49(3)
The association between dermatomyositis and polyradiculoneuritis is rarely citated in the speciality literature. Our patient had at first a disorder that looked like dermatomyositis, then she associated polyradiculoneuritis. At the presentation to ou
Autor:
T, Răşanu, Mihaela, Mehedinţi-Hâncu, Marilena, Alexianu, T, Mehedinţi, Emma, Gheorghe, Irene, Damian
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 53(1)
We present the case of a female patient, aged 12 years, with fatigability and exertional myalgias, progressively developed within the last two years. Negative family history, as well as negative personal medical history, were found. At physical exami