Results 81 to 90 of about 80,512 (251)

Deforestation and Efficiency: Insights From Forest Transition in the Brazilian Cerrado

open access: yesAgribusiness, EarlyView.
ABSTRACT This paper estimates technical efficiency (TE) and environmental efficiency (EE) of agricultural production at the municipal level of the Brazilian Cerrado in 2006 and 2017, and investigates their underlying mechanisms in relation to forest transition theory.
Ricardo Muniz Simões   +2 more
wiley   +1 more source

Radiology in Posterior Fossa Tumors

open access: yes, 2017
Posterior kranial fossa supratentoryal alana göre oldukça kısıtlı bir hacme sahiptir. İçinde yaşamsal merkezler ile tüm motor ve duyusal traktusları barındıran beyin sapını; 3.
Osman Kızılkılıç, Cem Çallı
core  

Malformations of the Posterior Fossa

open access: yes, 2016
Malformations of the posterior fossa include multiple entities which have been described in the recent years using different terminologies, thus causing some confusion in the literature about this topic.
Pasquale Capuano   +3 more
core   +1 more source

Spontaneous posterior fossa hemorrhage: profile and functional outcome in patients attending Tanta stroke unit

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery
Background The most dangerous and least curable type of stroke is spontaneous intracerebral hemorrhage (ICH), and prognosis is highly correlated with location and size in the posterior fossa.
Mahmoud Hamed Nassar   +5 more
doaj   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli   +18 more
wiley   +1 more source

Posterior fossa meningioma (surgical experiences)

open access: yes, 2013
IntroductionMeningioma is a common tumor that represents about 30% of all intracranial tumors. Posterior fossa location of the tumor is uncommon. It can be classified according to the location in the posterior fossa into cerebellopontine angle, clival ...
Moussa, Wael M., Naggar, Alaa El
core   +1 more source

Resolution of Refractory Multifocal Atrial Tachycardia in Costello Syndrome Using Trametinib: A Case Supporting MEK Inhibitors as Targeted, Specific Antiarrhythmic

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Arrhythmias affect approximately half of patients with Costello syndrome (CS, OMIM # 218040), with non‐reentrant atrial tachycardia being the most common. This case describes an infant with Costello syndrome carrying the pathogenic HRAS c.34G>A (p.G12S) variant who developed early‐onset, drug‐refractory multifocal atrial tachycardia (MAT ...
Vanina Taliercio   +11 more
wiley   +1 more source

Transpetrosal approaches to the posterior fossa

open access: yes, 2005
Resection of the petrous temporal bone to various degrees provides different levels of access to lesions of the posterior fossa. Although their nomenclature can be confusing, the numerous variants of the transpetrosal approaches can be classified broadly
Coscarella, Ernesto   +5 more
core   +1 more source

Morphometric Analysis of the Posterior Fossa and Cervical Spinal Canal in Type 1 Chiari Malformation and Its Effects on Syringomyelia Development

open access: yesİstanbul Medical Journal
Introduction: Chiari malformation (CIM) is a congenital anomaly characterized by herniation of hindbrain structures through the foramen magnum into the cervical spinal canal (CSC).
Tahsin Saygı   +2 more
doaj   +1 more source

Refining Domain‐Based Prognostication in DNM1 Encephalopathy: A Mild Phenotype Associated With a GTPase Domain Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain   +6 more
wiley   +1 more source

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