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8021
A Peripheral Ameloblastic Fibro-Odontoma in a 3-Year-Old Girl: Case Report, Immunohistochemical Analysis, and Literature Review
Published 2014-01-01“…Because this lesion clinically resembles other nonneoplastic lesions and is very rare in gingiva, establishing a correct diagnosis is achieved only based on specific histological characteristics. …”
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8022
Misdiagnosis: Acute Chest Syndrome That Evolved into Acute Respiratory Distress Syndrome in a Patient without a Documented History of Hemoglobinopathy
Published 2019-01-01“…Here is a case of a patient who presented with symptoms suggestive of acute chest syndrome yet had a delayed diagnosis presumably due to the lack of documented history of sickle cell disease of the patient, consequently evolving into acute respiratory distress syndrome (ARDS). …”
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8023
Tongue Necrosis Secondary to Giant Cell Arteritis: A Case Report and Literature Review
Published 2017-01-01“…Although unusual as an initial manifestation, tongue necrosis is an important alert for diagnosing giant cell arteritis. Early diagnosis and treatment of this atypical manifestation may reduce morbidity.…”
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8024
Survival Following Extreme Hypernatraemia Associated with Severe Dehydration and Undiagnosed Diabetes Mellitus
Published 2019-01-01“…The aetiology was believed to be due to severe dehydration and a new diagnosis of diabetes mellitus. Extreme hypernatraemia (serum sodium level greater than 190 mmol/L) is rare and associated with a high mortality. …”
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8025
Fetal sirenomelia type VI. A case report
Published 2025-01-01“…For these reasons, a 42-years-old pregnant patient with 17.5 weeks' gestational age and an ultrasound diagnosis of sirenomelia is presented, referred to the Dr. …”
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8026
Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet–Biedl Syndrome
Published 2022-01-01“…In this study, we used whole-exome sequencing (WES) to investigate the underlying mutations in four Iranian children from consanguineous families with a clinical diagnosis of Bardet–Biedl syndrome (BBS). In three out of four children, we identified one previously reported frameshifting variant in the BBS12 gene (c.265-266delTT, p.L89fs) and two novel nonsense variants in MKKS (c.1196T>G, p.L399X) and BBS7 genes (c.1636C>T, p.Q546X). …”
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8027
Hereditary colorectal cancer: genetics and screening diagnostics
Published 2018-08-01“…Both clinical and molecular genetic investigations of hereditary CRC forms make possible individual comprehensive approach for diagnosis verification, evaluation of cancer risk, early diagnostics, treatment and prevention for decrease of morbidity and mortality.…”
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8028
Atypical Presentation of Lemierre’s Syndrome Causing Septic Shock and Acute Respiratory Distress Syndrome
Published 2018-01-01“…Blood culture showed Fusobacterium, and antibiotics were changed accordingly following which there was a clinical improvement. The diagnosis of Lemierre’s syndrome was then established based on her presenting age and bilateral pulmonary empyema in the setting of septicemia with Fusobacterium.…”
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8029
Prevention of Cerebral Embolism Progression by Emergency Surgery of the Left Atrial Myxoma
Published 2015-01-01“…Cardiac myxoma is often associated with a high risk of embolic episodes, which emphasizes the need for prompt surgical excision as soon as the diagnosis is confirmed.…”
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8030
A Case of Misdiagnosed Cesarean Scar Pregnancy with a Viable Birth at 28 Weeks
Published 2014-01-01“…In the latter type, the gestational sac moves upward with increasing gestational weeks and it shows the same ultrasound image as a normal pregnancy. Therefore, the diagnosis must be made in the early pregnancy.…”
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8031
Predicting Intensive Care Unit Admissions in COVID-19 Patients: An AI-Powered Machine Learning Model
Published 2025-01-01“…Our algorithm examines several clinical and demographic characteristics to identify high-risk individuals early in illness diagnosis. We used 4399 patients to identify ICU admission with predictors such as shortness of breath, high D-dimer values, and abnormal chest X-rays. …”
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8032
Artifactual Hypoglycaemia in Systemic Sclerosis and Raynaud’s Phenomenon: A Clinical Case Report and Short Review
Published 2016-01-01“…Treatment of low capillary blood glucose is usually met with clinical impetus to treat, even when hypoglycaemic symptoms are lacking. The correct diagnosis may have been achieved had there been an observation of her cold hands, scleroderma facies, and consideration of the likely distorted peripheral microvasculature. …”
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8033
Simulation and Optimization of Bus Interior Noise Based on Hybrid Method for Engine Vibration Load Identification
Published 2024-01-01“…The primary causes of the interior booming noise were identified by simulation analysis and experimental diagnosis. Optimization analysis led to a notable noise reduction by adjusting the support stiffness of the drive shaft, body structure, and integrating rear leaf spring dampers. …”
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8034
Carp Edema Virus Disease (CEVD) / Koi Sleepy Disease (KSD)
Published 2015-12-01“…This 6-page fact sheet describes symptoms, diagnosis, prevention, and what fish producers, wholesalers, or retailers can do if they suspect carp may have contracted the disease. …”
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8035
Bilateral Facial Paralysis Caused by Bilateral Temporal Bone Fracture: A Case Report and a Literature Review
Published 2015-01-01“…Therefore, delays may ensue in both diagnosis and treatment of bilateral facial paralysis.…”
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8036
COVID-19 pandemic and its psychological impact among healthy Portuguese and Spanish nursing students
Published 2021-06-01“…Students with high perceived stress most likely had a COVID-19 diagnosis in their household; their household income had been affected by the COVID-19 pandemic; experienced difficulty falling asleep or sleeping all night; consumed junk food in excess; neglected their appearance; felt headaches, stomach aches, and back pain; and lacked the patience or desire to exercise. …”
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8037
Distance-Ranked Fault Identification of Reconfigurable Hardware Bitstreams via Functional Input
Published 2014-01-01“…For MCNC benchmark circuits, the observed reduction in input evaluations is up to 75% when comparing the DRFI technique to unguided evaluation. The DRFI diagnosis method is seen to isolate all 14 healthy configurations from a pool of 100 pregenerated configurations, and thereby offering a 100% isolation accuracy provided the fault-free configurations exist in the design pool. …”
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8038
Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system
Published 2024-10-01“…Multiple scoring systems have been identified, and previous approaches for CH assessment and reporting in genetic diagnosis have shown inconsistencies. Owing to the current heterogeneity in the classification of CHs, data analysis may be biased, impacting the quality of clinical reports and human genetic research. …”
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8039
Intravitreal Ampicillin Sodium for Antibiotic-Resistant Endophthalmitis: Streptococcus uberis First Human Intraocular Infection Report
Published 2010-01-01“…To describe the clinical characteristics, diagnosis, and treatment with intravitreal ampicillin sodium of a postoperative endophthalmitis case due to Streptococcus uberis; an environmental pathogen commonly seen in mastitis cases of lactating cows. …”
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8040
À propos de deux cas de brucellose dans le sud de la France aux époques médiévale et moderne (Abbaye Saint-Sauveur, Aniane ; La Closeraie, Aix-en-Provence)
Published 2022-02-01“…This is due to the rather complex differential diagnosis of the disease, in particular involving other infections with a predilection for the spine which were very frequent in past populations. …”
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