Results 51 to 60 of about 10,835,507 (313)

Empty nose syndrome : case report [PDF]

open access: yes, 2013
Empty Nose Syndrome (ENS) is a term first introduced by Kern and Moore which is used to describe a rare spectrum of various symptoms suffered by patients who had had previous radical turbinate surgery with a CT scan appearance of the paranasal sinuses ...
Aboud, Saleh Khaled, Aziz, Aini AB
core  

Sirolimus for Extracranial Arteriovenous Malformations: A Scoping Review of the Evidence in Syndromic and Non‐Syndromic Cases

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Arteriovenous malformations (AVMs) are rare, high‐flow, vascular anomalies that can occur either sporadically or as part of a genetic syndrome. AVMs can progress with serious morbidity and even mortality if left unchecked. Sirolimus is an mTOR inhibitor that is effective in low‐flow vascular malformations; however, its role in AVMs is unclear.
Will Swansson   +3 more
wiley   +1 more source

Flexor hallucis longus rupture repaired with split flexor digitorum longus tendon transfer: A case report

open access: yesFoot & Ankle Surgery: Techniques, Reports & Cases, 2021
Isolated rupture of the flexor hallucis longus tendon is an injury rarely reported in literature. In this case report, a 47-year-old female presented 3 months after traumatic injury which resulted in rupture of the flexor hallucis longus.
Jake Eisenschink, DPM   +2 more
doaj   +1 more source

Amyand’s hernia : a case report [PDF]

open access: yes, 2013
The presence of vermiform appendix, whether normal or inflamed in the inguinal hernia, is referred to as Amyand’s hernia. This is rare occurring in about 1% of inguinal hernias in adults.
Muscat, Peter
core  

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski   +9 more
wiley   +1 more source

Infantile Osteopetrosis in Two Siblings: Case Report

open access: yesDiyala Journal of Medicine, 2019
Case ...
Saad Sh Rajab, Omar K Khattab
doaj   +2 more sources

Pregnancy-Associated Osteoporosis: Case Report - Case Report

open access: yesTürk Osteoporoz Dergisi, 2006
Pregnancy associated osteoporosis is a rare complication manifested with back, low back pain after gestation, or in lactation period. The entity has been first described by Nordin and Roper in 1955.
Gülriz Özbek   +6 more
doaj  

Pyolaryngocele: Case report

open access: yesInternational Journal of Surgery Case Reports, 2023
Pyolaryngocele is a very rare and serious complication of laryngocoele. The clinical presentation can be extremely severe acute epiglottitis with laryngeal dyspnea and major dysphagia. The treatment of choice is surgical excision. Our aim is to attract the intention of the surgeon to this unusual entity and describe its clinical features.We report a ...
Touihmi, Safaa   +2 more
openaire   +2 more sources

Necrotising fasciitis : a case report [PDF]

open access: yes, 2013
Necrotising fasciitis is a rapidly progressive and potentially lifethreatening bacterial infection involving the subcutaneous tissues and fascia which can result in extensive tissue necrosis and severe sepsis.
Vella Critien, Rachel
core  

Intravitreal GD2‐Specific Chimeric Antigen Receptor T‐Cell Therapy for Refractory Retinoblastoma

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Effective treatments for advanced, treatment‐resistant retinoblastoma (RB) remain limited. GD2‐specific chimeric antigen receptor (CAR) T cells show potent antitumor activity with minimal toxicity but have not previously been evaluated in RB.
Subongkoch Subhadhirasakul   +13 more
wiley   +1 more source

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