Zobrazeno 1 - 10
of 819
pro vyhledávání: '"11"'
Autor:
Hatice Koçak Eker
Publikováno v:
Child's Nervous System. 37:1779-1784
Fronto-ocular syndrome (FOS) is a rarely seen trigonocephaly syndrome in which metopic synostosis features are unique. This report presents six cases with FOS. Clinical manifestations mainly involve skull and facial findings. Nearly all patients have
Publikováno v:
World Neurosurgery. 125:e937-e946
Objective Immediate postoperative and early clinical outcome of treatment of spinal kyphoscoliosis (SKS) associated with Chiari formation (CF) and syringomyelia (SM) and treated by atlantoaxial fixation is described. Methods During the period April 2
Publikováno v:
Braindevelopment. 37(5)
Glutaric aciduria type-1 (GA-1) is a disorder of amino acid metabolism. The usual clinical-onset is an acute encephalopathic crisis in early childhood. There are only a few cases diagnosed in older age groups. MRI features of the disease are well def
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 30(2)
Neuromuscular scoliosis is a challenging pathology to treat with high incidence of complications and failure of surgical fusion. Surgical correction can entail long fusion constructs extending to the pelvis. We report our experience in the use of bon
Autor:
Erwin M. J. Cornips, Rick Abbott, Lawrence B. Daniels, Rahul Gupta, Mostafa El Khashab, Adam L. Sandler, Sandeep Mohindra, Dominic Thompson, Farideh Nejat, Reza Yassari, Arundhati Biswas, Eliezer Kolatch, James T. Goodrich, Jasper van Aalst
Publikováno v:
Child's Nervous System, 29(1), 105-117. Springer
Positioned anatomically between the spinal epidural space and the intramedullary compartment, the spinal subdural space remains the least common area of localized infection in the central nervous system. Infectious processes of the subdural spinal sp
Autor:
Stephen C. Cunnane, Jennifer Tremblay-Mercier, Mélanie Plourde, M'hamed Bentourkia, Fabien Pifferi, Sébastien Tremblay
Publikováno v:
Epilepsia
Epilepsia, Wiley, 2008, 49, pp.76-79. ⟨10.1111/j.1528-1167.2008.01842.x⟩
Epilepsia, 2008, 49, pp.76-79. ⟨10.1111/j.1528-1167.2008.01842.x⟩
Epilepsia, Wiley, 2008, 49, pp.76-79. ⟨10.1111/j.1528-1167.2008.01842.x⟩
Epilepsia, 2008, 49, pp.76-79. ⟨10.1111/j.1528-1167.2008.01842.x⟩
Changes in the metabolism of polyunsaturated fatty acids (PUFA), both in children on the high fat ketogenic diet (KD) for seizure control and in rats on a KD enriched in PUFA, raise the possibility that increased brain arachidonic acid (ARA) and/or d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89b051033153f304df7e162e256e2876
https://hal.archives-ouvertes.fr/hal-02310287
https://hal.archives-ouvertes.fr/hal-02310287
Autor:
Ludovico D'Incerti, M. Morbin, Laura Verga, Maria Grazia Bruzzone, Nardo Nardocci, Laura Farina, G. Zorzi, Mario Savoiardo
Publikováno v:
Neuroradiology. 41(5)
We report the imaging findings in 11 patients with infantile neuroaxonal dystrophy. Ten patients underwent 15 MRI examinations; one patient had only CT. Of the ten patients who underwent MRI, eight had cerebellar atrophy and mildly increased signal f
Autor:
Shoji Tsuji, N N Nikolskaya, Markova Ed, H. Tanaka, Irina A. Ivanova-Smolenskaya, Sergey N. Illarioshkin
Publikováno v:
Annals of neurology. 40(1)
We examined a large family in which an X-linked recessive congenital ataxia manifested in 7 males from three generations. The affected boys first exhibited a marked delay of early developmental motor milestones. A neurological syndrome became evident
Autor:
Sho Okamoto, Kinya Yokoyama, Kuniaki Tanahashi, Atsushi Natsume, Takashi Izumi, Toshihiko Wakabayashi, Masaki Sumitomo, Masahiro Nishihori, Kenji Uda, Yoshio Araki, Takashi Mamiya, Fumiaki Kanamori
Publikováno v:
World Neurosurgery. 139:e325-e334
Cerebral revascularization surgery has been established as an effective treatment for moyamoya disease. On the other hand, harvesting grafts and tissues to nourish the scalp may increase the risk of postoperative wound-related complications. The purp
Autor:
Mari Yoshida, Teppei Komatsu, Monika Bradl, Kiyotaka Nakamagoe, Tatsuro Misu, Ichiro Nakashima, Masashi Aoki, Hiroshi Kuroda, Kazuo Fujihara, Koichi Narikawa, Hiroyoshi Suzuki, Toshimasa Ikeda, Hans Lassmann, Hiroya Nishida, Kimihiko Kaneko, Takashi Komori, Morinobu Seki, Yoshiki Takai, Shuhei Nishiyama, Hirohiko Ono, Norio Chihara, Satoko Tsuchida, Toshiyuki Takahashi
Publikováno v:
Brain. 143:1431-1446
Conformation-sensitive antibodies against myelin oligodendrocyte glycoprotein (MOG) are detectable in patients with optic neuritis, myelitis, opticomyelitis, acute or multiphasic disseminated encephalomyelitis (ADEM/MDEM) and brainstem/cerebral corti