| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Keun-Hwa Jung, Kon Chu, Soon-Tae Lee, Hee-Kwon Park, Dong-Hyun Kim, Jin-Hee Kim, Jae-Jun Bahn, Eun-Cheol Song, Manho Kim, Sang Kun Lee, Jae-Kyu Ro. Circulating endothelial progenitor cells as a pathogenetic marker of moyamoya disease. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. vol 28. issue 11. 2008-11-18. PMID:18612318. |
moyamoya disease (mmd) is an unusual form of chronic cerebrovascular occlusive disease that involves the formation of characteristically abnormal vessels. |
2008-11-18 |
2023-08-12 |
human |
| Nobuyuki Mori, Yukio Miki, Ken-ichiro Kikuta, Yasutaka Fushimi, Tsutomu Okada, Shin-ichi Urayama, Nobukatsu Sawamoto, Hidenao Fukuyama, Nobuo Hashimoto, Kaori Togash. Microbleeds in moyamoya disease: susceptibility-weighted imaging versus T2*-weighted imaging at 3 Tesla. Investigative radiology. vol 43. issue 8. 2008-08-21. PMID:18648257. |
to prospectively evaluate differences in detectability of cerebral microbleeds (mbs) in moyamoya disease (mmd) on susceptibility-weighted imaging (swi) and t2*-weighted imaging (t2*wi) at 3 t. |
2008-08-21 |
2023-08-12 |
Not clear |
| K Kikut. Experiences using 3-tesla magnetic resonance imaging in the treatment of Moyamoya disease. Acta neurochirurgica. Supplement. vol 103. 2008-07-10. PMID:18496957. |
to introduce our initial experiences using 3-tesla (3t) magnetic resonance (mr) imaging in the treatment of moyamoya disease (mmd). |
2008-07-10 |
2023-08-12 |
Not clear |
| Marcus Czabanka, Pablo Peña-Tapia, Gerrit A Schubert, Johannes Woitzik, Peter Vajkoczy, Peter Schmiede. Characterization of cortical microvascularization in adult moyamoya disease. Stroke. vol 39. issue 6. 2008-07-03. PMID:18403740. |
increased cortical microvascularization has been proposed to be a moyamoya disease (mmd)-specific characteristic. |
2008-07-03 |
2023-08-12 |
Not clear |
| Y Mineharu, W Liu, K Inoue, N Matsuura, S Inoue, K Takenaka, H Ikeda, K Houkin, Y Takagi, K Kikuta, K Nozaki, N Hashimoto, A Koizum. Autosomal dominant moyamoya disease maps to chromosome 17q25.3. Neurology. vol 70. issue 24 Pt 2. 2008-06-13. PMID:18463369. |
moyamoya disease (mmd) is an idiopathic steno-occlusive cerebrovascular disease that represents an important cause of stroke. |
2008-06-13 |
2023-08-12 |
Not clear |
| Sabrina Rüggeberg, Peter Horn, Xinping Li, Peter Vajkoczy, Thomas Fran. Detection of a gamma-carboxy-glutamate as novel post-translational modification of human transthyretin. Protein and peptide letters. vol 15. issue 1. 2008-05-09. PMID:18221012. |
during analysis of the proteome in the cerebrospinal fluid (csf) of the caucasian form of moyamoya disease (mmd), a novel post-translational modification of human transthyretin was observed. |
2008-05-09 |
2023-08-12 |
human |
| Anand Veeravagu, Raphael Guzman, Chirag G Patil, Lewis C Hou, Marco Lee, Gary K Steinber. Moyamoya disease in pediatric patients: outcomes of neurosurgical interventions. Neurosurgical focus. vol 24. issue 2. 2008-04-10. PMID:18275292. |
neurosurgical interventions for moyamoya disease (mmd) in pediatric patients include direct, indirect, and combined revascularization procedures. |
2008-04-10 |
2023-08-12 |
Not clear |
| b' D Vranjesevi\\xc4\\x87, N Jovi\\xc4\\x87, D Milovanovi\\xc4\\x87, A Djuki\\xc4\\x8. [Unilateral moyamoya disease associated with acrofacial vitiligo in a 13-year-old patient--case report]. Srpski arhiv za celokupno lekarstvo. vol 122. issue 7-8. 2008-01-08. PMID:17974397.' |
cerebrovascular moyamoya disease (mmd) is a clinical entity characterized by stenotic or occlusive lesions around the terminal portions of the internal carotid arteries (ica) and the formation of abnormal vascular networks at the base or convexity. |
2008-01-08 |
2023-08-12 |
Not clear |
| Dal-Soo Kim, Seok-Gu Kang, Do-Sung Yoo, Pil-Woo Huh, Kyoung Suok Cho, Chun Kun Par. Surgical results in pediatric moyamoya disease: angiographic revascularization and the clinical results. Clinical neurology and neurosurgery. vol 109. issue 2. 2007-04-03. PMID:16872739. |
we retrospectively reviewed the pediatric patients with moyamoya disease (mmd) who underwent bypass surgery at our institution to compare the surgical results according to the surgical procedures. |
2007-04-03 |
2023-08-12 |
Not clear |
| Yasushi Takagi, Ken-Ichiro Kikuta, Kazuhiko Nozaki, Motoaki Fujimoto, Junya Hayashi, Hirotoshi Imamura, Nobuo Hashimot. Expression of hypoxia-inducing factor-1 alpha and endoglin in intimal hyperplasia of the middle cerebral artery of patients with Moyamoya disease. Neurosurgery. vol 60. issue 2. 2007-04-03. PMID:17290185. |
moyamoya disease (mmd) is a cerebrovascular occlusive disease characterized by progressive stenosis or occlusion at the distal ends of the bilateral internal arteries. |
2007-04-03 |
2023-08-12 |
Not clear |
| Yasushi Takagi, Ken-ichiro Kikuta, Kazuhiko Nozaki, Nobuo Hashimot. Histological features of middle cerebral arteries from patients treated for Moyamoya disease. Neurologia medico-chirurgica. vol 47. issue 1. 2007-03-16. PMID:17245006. |
moyamoya disease (mmd) is a cerebrovascular occlusive disease characterized by progressive stenosis or occlusion at the distal ends of the bilateral internal carotid arteries. |
2007-03-16 |
2023-08-12 |
human |
| Ho Jun Seol, Kyu-Chang Wang, Seung-Ki Kim, Yong-Seung Hwang, Ki Joong Kim, Byung-Kyu Ch. Familial occurrence of moyamoya disease: a clinical study. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 22. issue 9. 2007-02-12. PMID:16565850. |
we reviewed a consecutive series of moyamoya disease (mmd) in children and studied their familial pedigrees to determine whether they showed specific clinical features or patterns of inheritance, and to investigate any correlation between familial mmd and common asian diseases. |
2007-02-12 |
2023-08-12 |
Not clear |
| Myung-Kul Yum, A-Young Oh, Hyo-Min Lee, Chong-Sung Kim, Seong-Deok Kim, Young-Sun Lee, Kyu-Chang Wang, You-Nam Chung, Hee-Soo Ki. Identification of patients with childhood moyamoya diseases showing temporary hypertension after anesthesia by preoperative multifractal Hurst analysis of heart rate variability. Journal of neurosurgical anesthesiology. vol 18. issue 4. 2006-11-07. PMID:17006118. |
this study was performed to determine whether the preoperative multifractal hurst analysis of heart rate variability might identify and characterize childhood patients with moyamoya disease (mmd) who showed temporary postoperative hypertension. |
2006-11-07 |
2023-08-12 |
Not clear |
| Yasushi Takagi, Ken-ichiro Kikuta, Nobutake Sadamasa, Kazuhiko Nozaki, Nobuo Hashimot. Caspase-3-dependent apoptosis in middle cerebral arteries in patients with moyamoya disease. Neurosurgery. vol 59. issue 4. 2006-10-27. PMID:17038954. |
moyamoya disease (mmd) is a cerebrovascular occlusive disease characterized by progressive stenosis or occlusion at the distal ends of bilateral internal arteries. |
2006-10-27 |
2023-08-12 |
Not clear |
| Michael E Kelly, Teresa E Bell-Stephens, Michael P Marks, Huy M Do, Gary K Steinber. Progression of unilateral moyamoya disease: A clinical series. Cerebrovascular diseases (Basel, Switzerland). vol 22. issue 2-3. 2006-10-06. PMID:16685122. |
the natural history of unilateral moyamoya disease (mmd) in adult patients is not clearly described in the literature. |
2006-10-06 |
2023-08-12 |
Not clear |
| Y Mineharu, K Takenaka, H Yamakawa, K Inoue, H Ikeda, K-I Kikuta, Y Takagi, K Nozaki, N Hashimoto, A Koizum. Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprinting. Journal of neurology, neurosurgery, and psychiatry. vol 77. issue 9. 2006-08-22. PMID:16788009. |
although the aetiology of moyamoya disease (mmd) has not been fully clarified, genetic analysis of familial mmd (f-mmd) has considerable potential to disclose it. |
2006-08-22 |
2023-08-12 |
Not clear |
| Ho Jun Seol, Kyu-Chang Wang, Seung-Ki Kim, Chang Sub Lee, Dong Soo Lee, In-One Kim, Byung-Kyu Ch. Unilateral (probable) moyamoya disease: long-term follow-up of seven cases. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 22. issue 2. 2006-07-06. PMID:16220301. |
some cases of unilateral involvement have angiographic findings on the affected side which resemble those of definite cases of moyamoya disease (mmd). |
2006-07-06 |
2023-08-12 |
Not clear |
| Ken Ikeda, Yasuo Iwasaki, Hidetoshi Kashihara, Ken-Ichi Hosozawa, Kouzo Anan, Masaki Tamura, Eijiro Satoyoshi, Hidetoshi Iked. Adult moyamoya disease in the asymptomatic Japanese population. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 13. issue 3. 2006-07-06. PMID:16540331. |
moyamoya disease (mmd) is a spontaneous occlusive disease of the willis circle. |
2006-07-06 |
2023-08-12 |
human |
| Mariko L Ishimori, Stanley N Cohen, David S Hallegua, Franklin G Moser, Michael H Weisma. Ischemic stroke in a postpartum patient: understanding the epidemiology, pathogenesis, and outcome of Moyamoya disease. Seminars in arthritis and rheumatism. vol 35. issue 4. 2006-06-19. PMID:16461070. |
moyamoya disease (mmd), or spontaneous occlusion of blood vessels in the circle of willis, is a noninflammatory, nonatheromatous vasculopathy that often presents with ischemia or hemorrhage and has a tendency to affect young women. |
2006-06-19 |
2023-08-12 |
Not clear |
| Ken-ichiro Kikuta, Yasushi Takagi, Yoshiki Arakawa, Susumu Miyamoto, Nobuo Hashimot. Absence epilepsy associated with moyamoya disease. Case report. Journal of neurosurgery. vol 104. issue 4 Suppl. 2006-05-02. PMID:16619638. |
the authors present the case of a 6-year-old girl with typical absence epilepsy induced by hyperventilation associated with moyamoya disease (mmd). |
2006-05-02 |
2023-08-12 |
Not clear |