Search results for "croce"
showing 10 items of 170 documents
Una correspondencia de doce años. Benedetto Croce y Giovanni Papini
2015
El presente texto pretende dar una muestra de la copleja relación epistolar que mantuvieron durante algo más de una década Benedetto Croce y Giovanni Papini, desde 1902 hasta 1914.
Croce, la religión y el cristianismo
2015
Los estudios centrados en la presencia del cristianismo en la filosofía de B. Croce han cobrado recientemente un gran impulso, cuestionando en muchos casos su supuesta conversión al catolicismo. En este sentido, el artículo analiza la evolución del pensamiento de B. Croce, considerando que, aunque su sistema filosófico cambió sensiblemente en los últimos años de su vida, debido en gran parte a los dramáticos sucesos acaecidos durante la II Guerra Mundial, Croce nunca renegó de su riguroso inmanentismo, evitando cualquier tipo de consuelo en el trascendentalismo. El autor propone, en esta línea, el estudio de los siguientes aspectos de la filosofía de Croce: La inmortalidad del alma y la pol…
Three rare lignicolous fungi from Sicily (S Italy)
2013
<em>Sarcodontia crocea</em> (Schwein.) Kotl., <em>Oligoporus mappa</em> (Overh. & Lowe) Gilbn. & Ryvarden and <em>Inonotus rickii</em> (Pat.) D.A. Reid. are reported for the first time from Sicily (southern Italy). Ecological and distributive features on the three relevant species are also here provided.
Perlman syndrome: Clinical report and nine-year follow-up
2005
We present the clinical and follow-up data of a female infant with Perlman syndrome from birth to the age of 9 years. Main features of Perlman syndrome include polyhydramnios, fetal overgrowth, neonatal macrosomia, macrocephaly, dysmorphic facial features, visceromegaly, nephroblastomatosis, and a predisposition for Wilm's tumor. In our patient, the nephromegaly with nephroblastomatosis was not present at birth or during the neonatal period; it became evident in the first months of postnatal life. A Wilm's tumor was diagnosed when she was about 1 year old. Long term follow-up documents the natural history of Perlman syndrome and allows us to establish the long-term prognosis of the affected…
LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters.
2019
Abstract Alazami syndrome (AS) (MIM# 615071 ) is an autosomal recessive microcephalic primordial dwarfism (PD) with recognizable facial features and severe intellectual disability due to depletion or loss of function variants in LARP7. To date, 15 patients with AS have been reported. Here we describe two consanguineous Algerian sisters with Alazami PD due to LARP7 homozygous pathogenic variants detected by whole exome sequencing. By comparing these two additional cases with those previously reported, we strengthen the key features of AS: severe growth restriction, severe intellectual disability and some distinguishing facial features such as broad nose, malar hypoplasia, wide mouth, full li…
A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14Mb microduplication in region 19q12
2011
A 9-year-old girl born to healthy parents showed manifestations suggestive of ataxia telangiectasia (AT), such as short stature, sudden short bouts of horizontal and rotary nystagmus, a weak and dysarthric voice, rolling gait, unstable posture, and atactic movements. She did not show several cardinal features typical of AT such as frequent, severe infections of the respiratory tract. In contrast, she showed symptoms not generally related to AT, including microcephaly, profound motor and mental retardation, small hands and feet, severely and progressively reduced muscle tone with slackly protruding abdomen and undue drooling, excess fat on her upper arms, and severe oligoarthritis. A cranial…
Pfeiffer syndrome: clinical and genetic findings in five Brazilian families
2014
Pfeiffer syndrome (PS) is mainly characterized by craniosysnostosis, midface hypoplasia, great toes with partial syndactyly of the digits and broad and medially deviated thumbs. It is caused by allelic mutations in the fibroblast growth factor receptor 1 and 2 (FGFR1 and 2) genes. This study describes the clinical and genetic features of five Brazilian families affected by PS. All patients exhibited the classical phenotypes related to PS. The genetic analysis was able to detect the mutations Cys278Phe, Cys342Arg, and Val359Leu in three of these families. Two mutations were de novo, with one familial. We identified pathogenic mutations in four PS cases in five Brazilian families by PCR seque…
La categoría de la vitalidad en el último Croce
2015
La divergencia entre realidad histórica e ideal moral, es decir, la lucha entre fuerzas vitales y fuerzas morales, es una de las preocupaciones fundamentales de la filosofía del último Croce. Para ello parte de una aguda crítica al extremo vitalismo que condujo a la II Guerra Mundial, considerado no como fuerza categorial del espíritu, sino como una fuerza identificable con la irracionalidad de puro impulso individual. En este contexto, cobra relevancia su pensamiento en torno a la religión y su relación con el estado, así como el descubrimiento del sufrimiento, o mejor dicho, de la ética como sufrimiento, que sustituye el previo “descubrimiento de lo útil” como otra y más profunda clave pa…
LA SFIDA DI MISTRETTA PER UNA RINASCITA CULTURALE ATTRAVERSO LA VALORIZZAZIONE DEL SUO PATRIMONIO STORICO-ARTISTICO
2012
una breve rassegna di suppellettili liturgiche restaurate appartenenti alla Chiesa Madre di Santa Lucia di Mistretta.
Contribution to the modeling of microstructural corrosion on aluminium alloys : definition of a methodology to study the bimetallic corrosion phenome…
2008
The initiation and the propagation of aluminum alloys microstructural corrosion is mainly based on the bimetallic corrosion phenomenon. This type of corrosion is caused by galvanic coupling at a local scale between the different phases contained in the alloy. The description of the localized corrosion phenomenon has been largely studied. Their complexity can explain why they are so difficult to predict by the way of numerical tools and why the works that have been done on this subject are so scarce. The present thesis brings a new contribution to this field by suggesting a methodology based on the complementary use of local electrochemical techniques and the finite element simulation of bim…