Results 81 to 90 of about 21,617 (225)

A 3D atlas of the trigeminal nerve and its relevance for comparative studies of the masticatory apparatus in rodents

open access: yesJournal of Anatomy, EarlyView.
The trigeminal nerve of the rat (Rattus norvegicus) and its relationship with different masticatory muscles. dig, digastric nerve; ep, external pterygoid nerve; ip, internal pterygoid nerve; maadm, branch of the masseteric nerve for the anterior deep masseter; mapdm, branches of the masseteric nerve for the posterior deep masseter; masm, branch of the ...
Lionel Hautier   +5 more
wiley   +1 more source

Patent foramen ovale may be causal for the first stroke but unrelated to subsequent ischemic events [PDF]

open access: yes, 2011
Studies with very long follow-up are scarce in patients with cryptogenic stroke and patent foramen ovale (PFO).
Arnold, Marcel   +27 more
core   +1 more source

Death by patent foramen ovale in a soccer player [PDF]

open access: yes, 2013
A 34-year-old male patient was referred for primary percutaneous coronary intervention for ST-segment elevation myocardial infarction with cardiogenic shock and was found to have embolic left coronary artery occlusion and subsegmental pulmonary artery ...
Khattab, Ahmed A.   +2 more
core  

Child health [PDF]

open access: yes, 2014
Contents: President’s address at the MMCFD graduation of vocational trainees, 25 March 2014 - Pierre Mallia; MMCFD Graduation Photos 25 March 2014The mission of the Journal of the Malta College of Family Doctors (JMCFD) is to deliver accurate ...
Mallia, Pierre   +2 more
core  

Gas exchange and pulmonary stress variations during SCUBA and breath‐hold diving in open seawater

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend Healthy, trained divers were studied before, during and after diving in open seawater with different techniques. SCUBA divers (diving to 15 or 40 m with air; cycling at depth) and breath‐hold divers (BHDs; sled‐assisted dives to 15, 25 or 40 m) underwent underwater and surface arterial blood gas (ABG) sampling.
Matteo Paganini   +11 more
wiley   +1 more source

Thrombus crossing through a patent foramen ovale [PDF]

open access: yes, 2009
Paradoxical embolism across a patent foramen ovale (PFO) is a rare clinical entity and the thrombus is rarely caught passing through a PFO. A 65-year-old woman presented with dyspnea and pleuritic chest pain.
DOĞAN, Ali   +5 more
core   +1 more source

Increased Risk of Sarcomas in Children With Congenital Anomalies: Findings From the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Registry Linkage Study

open access: yesPediatric Blood &Cancer, Volume 73, Issue 8, August 2026.
ABSTRACT Background Pediatric sarcomas are a heterogeneous group of tumors that contribute disproportionately to cancer mortality in children. Although congenital anomalies are among the strongest known risk factors for childhood cancer, the risk of specific sarcoma subtypes among affected individuals has not yet been thoroughly evaluated. Procedure We
Russ Wolters   +17 more
wiley   +1 more source

Identification of patent foramen ovale permitting paradoxic embolism [PDF]

open access: yes, 1995
Objectives.We sought to analyze the morphologic and functional characteristics of the patent foramen ovale in patients with different clinical likelihoods for paradoxic embolism.Background.The incidence of patent foramen ovale is increased in patients ...
Hausmann, Dirk   +2 more
core   +1 more source

Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying Severe Noonan Syndrome With Adult‐Onset Acute Myeloid Leukemia

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1879-1883, August 2026.
ABSTRACT Noonan syndrome (NS) is a genetically heterogeneous disorder characterized by a broad spectrum of clinical features resulting from dysregulation of the RAS/MAPK pathway. Although complex genotypes are increasingly recognized in NS, cases harboring two distinct pathogenic variants in different NS genes remain extremely rare.
Francesco Prevedello   +10 more
wiley   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1783-1798, August 2026.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

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