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BULLETIN OF THE WORLD HEALTH ORGANIZATION, ISSN 0042-9686, 10/2011, Volume 89, Issue 10, pp. 766 - 774
Objective To update the estimated global incidence of Japanese encephalitis (JE) using recent data for the purpose of guiding prevention and control efforts.... 
IMMUNIZATION | AUSTRALIA | SHANGHAI | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | MALAYSIA | DISEASE | SURVEILLANCE | CLINICAL-FEATURES | CHILDREN YOUNGER | OUTBREAK | BURDEN | Research
Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 2014, Volume 20, Issue 21, pp. 6364 - 6373
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 01/2011, Volume 74, Issue 1, pp. 9 - 20
Classical pituitary apoplexy is a medical emergency and rapid replacement with hydrocortisone maybe life saving. It is a clinical syndrome characterized by the... 
SURGERY | INFARCTION | HEMORRHAGE | RECOMMENDATIONS | ENDOCRINE | ENDOCRINOLOGY & METABOLISM | ADENOMA | IMPROVEMENT | PRECIPITATING FACTORS | CLINICAL-FEATURES | TUMOR APOPLEXY
Journal Article
Chronic actinic dermatitis - A study of clinical features, 12/2005
Background: Chronic actinic dermatitis (CAD), one of the immune mediated photo-dermatoses, comprises a spectrum of conditions including persistent light... 
Chronic actinic dermatitis, Clinical features
Journal
Profile of Behcet's disease at Van and Vicinity, 12/2005
Aim: Behcet's disease is a chronic, progressive disease with an unknown etiology and involves many organs and systems. Although the disease can be encountered... 
Behcet's disease, clinical features, Van
Journal
Canadian Journal of Ophthalmology/Journal canadien d'ophtalmologie, ISSN 0008-4182, 02/2020, Volume 55, Issue 1, pp. e36 - e39
Journal Article
The Pediatric infectious disease journal, ISSN 0891-3668, 2016, Volume 35, Issue 11, pp. 1277 - 1278
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 02/2018, Volume 138, Issue 2, pp. 265 - 272
Eczema herpeticum (EH) is characterized by viral infection of a preexisting inflammatory dermatosis and is associated with considerable morbidity. In this... 
ATOPIC-DERMATITIS | CLINICAL-FEATURES | STEVENS-JOHNSON-SYNDROME | DERMATOLOGY
Journal Article
by Northrup, Hope and Krueger, Darcy A and Roberds, Steven and Smith, Katie and Sampson, Julian and Korf, Bruce and Kwiatkowski, David J and Mowat, David and Nellist, Mark and Povey, Sue and de Vries, Petrus and Byars, Anna and Dunn, David and Ess, Kevin and Hook, Dena and Jansen, Anna and King, Bryan and Sahin, Mustafa and Whittemore, Vicky and Thiele, Elizabeth and Bebin, E. Martina and Chugani, Harry T and Crino, Peter and Curatolo, Paolo and Holmes, Greg and Nabbout, Rima and O'Callaghan, Finbar and Wheless, James and Wu, Joyce and Darling, Thomas N and Cowen, Edward W and Gosnell, Elizabeth and Hebert, Adelaide and Mlynarczyk, Greg and Soltani, Keyomaurs and Teng, Joyce and Wataya-Kaneda, Mari and Witman, Patricia M and Kingswood, Chris and Bissler, John and Budde, Klemens and Hulbert, John and Guay-Woodford, Lisa and Sauter, Matthias and Zonneberg, Bernard and Jóźwiak, Sergiusz and Bartels, Ute and Berhouma, Moncef and Franz, David Neal and Koenig, Mary Kay and Roach, E. Steve and Roth, Jonathan and Wang, Henry and Weiner, Howard and McCormack, Francis X and Almoosa, Khalid and Brody, Alan and Burger, Charles and Cottin, Vincent and Finlay, Geraldine and Glass, Jennifer and Henske, Elizabeth Petri and Johnson, Simon and Kotloff, Robert and Lynch, David and Moss, Joel and Smith, Karen and Rhu, Jay and Da Silva, Angelo Taveira and Young, Lisa R and Knilans, Timothy and Hinton, Robert and Prakash, Ashwin and Romp, Robb and Singh, Arun D and DebRoy, Ashish and Chen, Pei-Lung and Sparagana, Steven and Frost, Michael D and International Tuberous Sclerosis Complex Consensus Group and Int Tuberous Sclerosis Complex
Pediatric Neurology, ISSN 0887-8994, 2013, Volume 49, Issue 4, pp. 243 - 254
Abstract Background Tuberous sclerosis complex is highly variable in clinical presentation and findings. Disease manifestations continue to develop over the... 
Pediatrics | Neurology | tuberous sclerosis | diagnostic criteria | clinical features | LYMPHANGIOLEIOMYOMATOSIS | MANAGEMENT | VARIANTS | FUNCTIONAL ASSESSMENT | TSC1 | CARDIAC TUMORS | CLINICAL NEUROLOGY | MICRONODULAR PNEUMOCYTE HYPERPLASIA | ANGIOMYOLIPOMAS | DISEASE | HOGG-DUBE-SYNDROME | PEDIATRICS | Conferences, meetings and seminars | Tuberous sclerosis
Journal Article
Pain (Amsterdam), ISSN 0304-3959, 2014, Volume 155, Issue 4, pp. 654 - 662
Journal Article
by Wu, JH and Zhong, WW and Yin, Y and Zhang, H
BMC PEDIATRICS, ISSN 1471-2431, 11/2019, Volume 19, Issue 1, pp. 410 - 7
Background Primary immunodeficiency disease (PID) is a disorder caused by an inherited flaw in the immune system that increases the susceptibility to... 
Demographic characteristics | CELL TRANSPLANTATION | CLASSIFICATION | COMMITTEE | CLINICAL-FEATURES | PREVALENCE | Clinical features | INTERNATIONAL UNION | China | Primary immunodeficiency disease | PEDIATRICS | COMPLICATIONS | UPDATE | Children
Journal Article
EUROSURVEILLANCE, ISSN 1560-7917, 09/2013, Volume 18, Issue 38, pp. 7 - 10
The stability of Middle East respiratory syndrome coronavirus (MERS-CoV) was determined at 20 degrees C - 40% relative humidity (RH); 30 degrees C - 30% RH and... 
INFECTIOUS DISEASES | CLINICAL-FEATURES
Journal Article
Journal Article
Journal Article
Original Article - High prevalence of spinocerebellar ataxia type 1 in an ethnic Tamil community in India, 12/2005
Objective: To study the prevalence, clinical and molecular genetic characteristics of cerebellar ataxia in an ethnic Tamil community in India. Methods: An... 
prevalence | Clinical features | genetics | SCA1 | India
Journal