Results 31 to 40 of about 14,741 (259)

Normal Pressure Hydrocephalus [PDF]

, 2020
Normal pressure hydrocephalus (NPH) is characterized by dilated ventricles and a combination of gait impairment, cognition impairment, and loss of urinary control (urgency and incontinence).
Agrawal, Amit, Deora, Harsh, Keni, Ravish Rajiv   +2 more
core   +1 more source

Endoscopic third ventriculostomy in idiopathic normal pressure hydrocephalus

Alexandria Journal of Medicine, 2014
Objective: To determine the efficacy of endoscopic fenestration of the third ventricle in the treatment of idiopathic normal pressure hydrocephalus.
Mohammed Ahmed Eshra
doaj   +1 more source

Dual-task related gait changes after CSF tapping: a new way to identify idiopathic normal pressure hydrocephalus [PDF]

, 2013
BACKGROUND: Gait disturbances found in patients with idiopathic normal pressure hydrocephalus (iNPH) are unspecific to the diagnosis and commonly occur in neurodegenerative or vascular conditions (iNPH-like conditions).
Francois R Herrmann, Frederic Assal, Gilles Allali, Magali Laidet, Olivier Beauchet, Stephane Armand   +5 more
core   +2 more sources

Monro-Kellie 2.0: The dynamic vascular and venous pathophysiological components of intracranial pressure [PDF]

, 2016
For 200 years, the ‘closed box’ analogy of intracranial pressure (ICP) has underpinned neurosurgery and neuro-critical care. Cushing conceptualised the Monro-Kellie doctrine stating that a change in blood, brain or CSF volume resulted in reciprocal ...
Wilson, MH
core   +1 more source

Normal-pressure hydrocephalus: A critical review

Dementia & Neuropsychologia, 2019
. Normal-pressure hydrocephalus (NPH) is a potentially reversible syndrome characterized by enlarged cerebral ventricles (ventriculomegaly), cognitive impairment, gait apraxia and urinary incontinence.
Louise Makarem Oliveira, Ricardo Nitrini, Gustavo C. Román   +2 more
doaj   +1 more source

Noninvasive prediction of shunt operation outcome in idiopathic normal pressure hydrocephalus [PDF]

, 2015
Idiopathic normal pressure hydrocephalus (iNPH) is a syndrome characterized by gait disturbance, cognitive deterioration and urinary incontinence in elderly individuals.
Aoki, Yasunori, Canuet Delis, Leonides, Hata, Masahiro, Hiroaki, Kazui, Ikeda, Shunichiro, Imajo, Kaoru, Ishii, Ryouhei, Iwase, Masao, Kanemoto, Hideki, Matsuzaki, Haruyasu, Musha, Toshimitsu, Nomura, Keiko, Takeda, M., Themistoklis, Katsimichas, Toshihisa, Tanaka, Wada, Tamiki, Yoshida, Tetsuhiko, Yoshiyama, Kenji   +17 more
core   +3 more sources

Amyloid mis-metabolism in idiopathic normal pressure hydrocephalus [PDF]

, 2016
BACKGROUND: Patients with idiopathic normal pressure hydrocephalus (iNPH) have reduced cerebrospinal fluid (CSF) concentrations of amyloid-β (Aβ) and α- and β-cleaved soluble forms of amyloid precursor protein (sAPPα and sAPPβ).
Blennow, K, Höltta, M, Jeppsson, A, Tullberg, M, Wikkelsø, C, Zetterberg, H   +5 more
core   +1 more source

Familial idiopathic normal pressure hydrocephalus [PDF]

Fluids and Barriers of the CNS, 2015
Version of ...
Huovinen, Joel, Kastinen, Sami, Komulainen, Simo, Oinas, Minna, Avellan, Cecilia, Franzen, Janek, Rinne, Jaakko, Ronkainen, Antti, Kauppinen, Mikko, Lönroth, Kimmo, Perola, Markus, Pyykkö, Okko T, Koivisto, Anne M, Remes, Anne M, Hiltunen, Mikko, Helisalmi, Seppo, Kurki, Mitja, Jääskeläinen, Juha E, Leinonen, Ville   +18 more
openaire   +2 more sources

Venous hemodynamics in neurological disorders: an analytical review with hydrodynamic analysis. [PDF]

, 2013
Venous abnormalities contribute to the pathophysiology of several neurological conditions. This paper reviews the literature regarding venous abnormalities in multiple sclerosis (MS), leukoaraiosis, and normal-pressure hydrocephalus (NPH).
A Furuta, A Kutzelnigg, A Larsson, A Laupacis, A Minagar, A Tsunoda, AC Guyton, AF Frydrychowski, AG Kermode, AI Katz, AJ Wakefield, AM Shaaban, AW Varga, B Schaller, B Schlesinger, B Yamout, BF Popescu, BK Owler, C Baracchini, C Baracchini, C Beggs, C Krogias, C Magnano, CA Mayer, CB Beggs, CB Beggs, CH Tator, CJ Fowler, CK Lyon, CK Lyon, Clive B Beggs, CM Dalton, CM Dalton, CP Chung, CP Chung, CP Chung, CP Gilmore, CR Jack Jr, CR Thore, CW Adams, CW Adams, D Centonze, D Inzitari, D Inzitari, D Inzitari, D Inzitari, D Kidd, D Pitt, D San Millan Ruiz, D Utriainen, DG Talbert, DJ Brooks, DJ Werring, DM Moody, DM Moody, DM Moody, DP Briley, DS Kim, E Menegatti, E Mori, EC Tallantyre, EM Haacke, F Aboul-Enein, F Doepp, F Doepp, F Fazekas, F Schelling, G Schroth, GA Bateman, GA Bateman, GA Bateman, GA Bateman, GA Bateman, GA Bateman, GA Bateman, GA Bateman, GJ Hankey, GL Schwartz, H Kitagaki, H Lassmann, H Williams, H Williams, HE Hulst, HL Rekate, HM Duvernoy, HR Parvey, HS Markus, IL Tan, J De Keyser, J Ekstedt, J Helenius, J Kawamura, J Kawamura, J Kim, J Kirk, J Lycke, J Plumb, J Simon, J van Gijn, J Wuerfel, J Wuerfel, JA Sloane, JC van Swieten, JH Moyer, JJ Lochhead, JM Luce, JM McCormick, JN Higgins, JN Higgins, JP Holt, JR Vignes, JW Dawson, K Ambarki, KA Witt, KA Witt, L Monti, L Pantoni, M D'Haeseleer, M Egnor, M Egnor, M Fernandez, M Inglese, M Kiefer, M Kitano, M Kobari, M Law, M Mancini, M Mase, M O'Sullivan, M O'Sullivan, M Saito, M Simka, M Sospedra, M Tullberg, M Tullberg, M Wiszniewska, M Zaniewski, ME Wagshul, MG Benedetti, MH Al-Omari, MJ Taffoni, MP Wattjes, MP Wattjes, MS Fernando, N Alperin, ND Chiaravalloti, NP Young, NR Graff-Radford, O Algin, O Khan, P Gideon, P Sundstrom, P Zamboni, P Zamboni, P Zamboni, P Zamboni, P Zamboni, P Zamboni, P Zamboni, PH Luetmer, PJ Chai, R Martin, R Sakakibara, R Sakakibara, R Schmidt, R Ylikoski, R Zivadinov, R Zivadinov, RL Swank, RW Cutler, S Adhya, S Bastianello, S El Sankari, S Hakim, S Leech, S Momjian, T Fog, T Miyati, TJ Putnam, TJ Putnam, U Graumann, VH ten Dam, W Bruck, W Rashid, WC Olivero, WG Bradley, WG Bradley, WG Bradley Jr, WG Bradley Jr, WG Bradley Jr, WI McDonald, WP Dillon, WR Brown, WR Brown, WR Brown, WR Brown, X Sun, Y Ge, Y Ge, Y Ge, Y Ge, Y Ge, Y Nakahara   +202 more
core   +1 more source

Blake's pouch cyst-like imaging abnormalities in idiopathic normal pressure hydrocephalus

Brain Disorders
Objective: Blake's pouch cyst is a cause of congenital non-communicating hydrocephalus. Recent study revealed that adult onset communicating normal pressure hydrocephalus sometimes accompanied by Blake's pouch cyst-like imaging abnormalities.
Yumiko Saito, Toru Baba, Wataru Narita, Shigenori Kanno, Shunji Mugikura, Yasuko Tatewaki, Yoshiyuki Nishio, Osamu Iizuka, Yasuyuki Taki, Teiji Tominaga, Etsuro Mori, Kyoko Suzuki   +11 more
doaj   +1 more source