Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Irene, Damian"'
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:
Anca Hancu, Irene Damian, Steliana Popescu, Bogdan Horia Davidescu, Daniela Zguma, Cristina Hertea, Masud Kaivanifard
Publikováno v:
Romanian Journal of Neurology, Vol 8, Iss 3, Pp 109-114 (2009)
This study was performed on a group of 50 patients admitted in 2008 in the Neurology Department, Emergency Hospital Constanta, whose cerebral MRI revealed leukoaraiosis. Our purpose was to correlate leukoaraiosis with associated vascular pathologies.
Externí odkaz:
https://doaj.org/article/118525f4db4340c1a5e60be3761eace3
Publikováno v:
Romanian Journal of Neurology, Vol 8, Iss 1, Pp 11-17 (2009)
Although essential tremor (ET) is a common movement disorder, the neural mechanism underlying this condition remains unknown. Because no diagnostic pathologic findings or biologic markers are available, correct diagnosis often depends on the clinicia
Externí odkaz:
https://doaj.org/article/48ed27f5137b4d67ba0eeeb004f44165
Autor:
Irene Damian, N. Cârciumaru
Publikováno v:
Romanian Journal of Neurology, Vol 5, Iss 1, Pp 16-22 (2006)
O serie de observații recente susțin ideea potrivit căreia un deficit de factori neurotrofici ar putea contribui la producerea bolii neuronului motor, dacă acționează concomitent cu alte procese patogenice. Articolul prezintă de asemenea o sin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::334ecfebb4ce5f749907db5a51e06820
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2006-Nr.1/RJN_2006_1_Art-04.pdf
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2006-Nr.1/RJN_2006_1_Art-04.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::7bc8324b75835f4321a2223a711343b5
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2006-Nr.1/RJN_2006_1_Art-02.pdf
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2006-Nr.1/RJN_2006_1_Art-02.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::db8683a07191c30a30d4825c3639176b
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2005-Nr.3/RJN_2005_3_Art-03.pdf
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2005-Nr.3/RJN_2005_3_Art-03.pdf
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,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::5389a02e4f07426e765a1546f6a59218
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2005-Nr.3/RJN_2005_3_Art-02.pdf
https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2005-Nr.3/RJN_2005_3_Art-02.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e6c3641f9e3d3b9be748477fd5a24be
https://pubmed.ncbi.nlm.nih.gov/22395524
https://pubmed.ncbi.nlm.nih.gov/22395524