Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Goni, Merhav"'
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Background and objectivesPrimary CNS vasculitis (PCNSV) is a rare inflammatory disorder that affects the blood vessels of the central nervous system (CNS). We aimed to analyze the neurological presentations, clinical follow-up, and long-term outcomes
Externí odkaz:
https://doaj.org/article/1eefc6e731034362a6fad028163a74ee
Publikováno v:
Infectious Diseases. 53:231-240
Q fever osteoarticular infections are a rare complication of the chronic form of Q fever. We aimed to characterize chronic Q fever vertebral osteomyelitis through our experience and a review of the literature.Four adult patients with Q fever vertebra
Publikováno v:
Journal of Clinical Imaging Science
Objectives: The prevalence of thyroid nodules in adults, detected by ultrasound (US), is reported as high as 68%. US-guided fine-needle aspiration biopsy (FNAB) is the test of choice used to determine the nature of the nodules. However, not more than
Autor:
Nira Razi, Goni Merhav
Publikováno v:
Journal of Clinical Imaging Science
Objectives: Renal ultrasound (US) is widely used for diagnosing renal pathologies, though few of them, such as obstructive uropathy, require emergent urological intervention. During on-call hours, when medical staff is limited, it is important to pri
Autor:
Nina Ekhilevitch, Takeshi Mizuguchi, Kazuyuki Nakamura, Masami Togawa, Kazuhiro Ogata, Naomichi Matsumoto, Asako Horino, Hirotomo Saitsu, Yukihiro Ikeda, Mai Satoh, Goni Merhav, Yasunari Sakai, Momoko Sasazuki, Fumiaki Tanaka, Hiroyuki Torisu, Hidehisa Takahashi, Hiroshi Doi, Toshiro Hara, Mazumi Miura, Takuma Kumamoto, Shouichi Ohga, Chiaki Ohtaka-Maruyama, Atsushi Takata, Takabumi Miyama, Mitsuhiro Kato, Masataka Fukuoka, Hideyuki Asai, Hideyuki Takeuchi, Tatsuhiko Tsunoda, Hiroko Ikeda, Takaaki Matsui, Atsushi Suzuki, Yushi Noguchi, Nobusuke Kimura, Keisuke Hamada, Mitsuko Nakashima, Eriko Koshimizu, Fuyuki Miya, Kohei Hamanaka, Noriko Miyake, Satoko Miyatake, Nodoka Hinokuma, Tomonori Hirose, Yoko Nishimura, Akio Yamashita, Kaoru Amemiya, Masaki Miura, Yuri Sonoda, Kazunori Sasaki
Publikováno v:
Science Advances
ATP1A3, a mutated gene for AHC, RDP, and CAPOS, is also associated with polymicrogyria by different functional variants.
Polymicrogyria is a common malformation of cortical development whose etiology remains elusive. We conducted whole-exome seq
Polymicrogyria is a common malformation of cortical development whose etiology remains elusive. We conducted whole-exome seq
Publikováno v:
Quintessence international (Berlin, Germany : 1985). 51(6)
Necrotizing sialometaplasia is a benign, self-limiting, inflammatory disease of salivary glands, mainly involving the minor salivary glands in the palate. This lesion can mimic a malignant neoplasm, both clinically and histopathologically, manifestin