Results 31 to 40 of about 3,899,299 (203)
Cluster headache in Greece: an observational clinical and demographic study of 302 patients. [PDF]
, 2016 BackgroundCluster headache (CH) is considered the most excruciating primary headache syndrome; although much less prevalent than migraine, it is not rare as it affects more than 1/1000 people.
Rapoport, Alan M, Vikelis, Michail
core +1 more source
Clinical features and outcomes of adrenal schwannoma: a study of 13 cases from a single centre
Endocrine Connections, 2021 Background: Adrenal schwannomas (AS) are extremely rare neoplasms. This st udy shares our experience regarding the diagnosis and operative management of AS.
Henghai Huang +5 more
doaj +1 more source
Rett Syndrome: Revised diagnostic criteria and nomenclature [PDF]
, 2010 Objective: Rett syndrome (RTT) is a severe neurodevelopmental disease that affects approximately 1 in 10,000 live female births and is often caused by mutations in Methyl-CpG-binding protein 2 (MECP2). Despite distinct clinical features, the accumulation
Amir +24 more
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Clinical, epidemiological and virological features of acute hepatitis B in Italy [PDF]
, 2015 Purpose To evaluate the association of hepatitis B virus (HBV) genotypes, basal core promoter (BCP)/precore (PC) and S gene mutations with the clinical-epidemiological characteristics of acute hepatitis B (AHB) in Italy.
Alessandro Remo Zanetti +10 more
core +1 more source
Pakistan Armed Forces Medical Journal, 2023 Objective: To determine the etiological pattern, clinical presentation and outcome of patients with proptosis in a tertiary care hospital. Study Design: Cross-sectional study.
Syed Imad Zahir +4 more
doaj +1 more source
Post-Partum Pituitary Insufficiency and Livedo Reticularis Presenting a Diagnostic Challenge in a Resource Limited Setting in Tanzania: A Case Report, Clinical Discussion and Brief Review of Existing Literature. [PDF]
, 2012 Pituitary disorders following pregnancy are an important yet under reported clinical entity in the developing world. Conversely, post partum panhypopituitarism has a more devastating impact on women in such settings due to high fertility rates, poor ...
A Cénac +27 more
core +3 more sources
Clinical features of neuroferritinopathy
Rinsho Shinkeigaku, 2009 Neuroferritinopathy is an autosomal dominant basal ganglia disease with iron accumulation caused by a mutation of the gene encoding ferritin light polypeptide (FTL). Six pathogenic mutations in the FTL gene have so far been reported. One such mutation was found in a Japanese family, thus suggesting that a new mutation in the FTL gene can therefore ...
Emiko, Ohta +7 more
openaire +3 more sources
Advances in Clinical Neuroscience & RehabilitationVascular Parkisonism (VP) can result from infarction or haemorrhage in the nigrostriatal pathway or from small vessel disease in the white matter. Although it represents 2.5-5% of all Parkinsonism cases, VP is frequently misdiagnosed due to its ...
Ana Lukic, Rajinder Singh
doaj +1 more source
Norovirus infection in children in Romania [PDF]
Romanian Journal of PediatricsNorovirus represents the most frequent cause of pediatric gastroenteritis requiring medical care. We conducted a prospective study on 276 patients admitted to a tertiary hospital in Romania from January 2017 to December 2019 to estimate the clinic ...
Luminita Bajenaru +8 more
doaj +1 more source
A rare case of pediatric renal paraganglioma [PDF]
Jichu yixue yu linchuangObjective To explore the clinical characteristics of renal paraganglioma(PGL). Methods The clinical data of a rare case of renal paraganglioma in a pediatric patient were reported and published cases of renal paragangliomas both domestically and ...
ZHANG Wenqian, ZHOU Yue, TONG Anli
doaj +1 more source