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1.
Clin Genet ; 91(5): 780-786, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-27882542

RESUMO

We present three members of an Italian family affected by tubular aggregate myopathy (TAM) and congenital miosis harboring a novel missense mutation in ORAI1. All patients had a mild, late onset TAM revealed by asymptomatic creatine kinase (CK) elevation and congenital miosis consistent with a Stormorken-like Syndrome, in the absence of thrombocytopathy. Muscle biopsies showed classical histological findings but ultrastructural analysis revealed atypical tubular aggregates (TAs). The whole body muscle magnetic resonance imaging (MRI) showed a similar pattern of muscle involvement that correlated with clinical severity. The lower limbs were more severely affected than the scapular girdle, and thighs were more affected than legs. Molecular analysis revealed a novel c.290C>G (p.S97C) mutation in ORAI1 in all affected patients. Functional assays in both human embryonic kidney (HEK) cells and myotubes showed an increased rate of Ca2+ entry due to a constitutive activation of the CRAC channel, consistent with a 'gain-of-function' mutation. In conclusion, we describe an Italian family harboring a novel heterozygous c.290C>G (p.S97C) mutation in ORAI1 causing a mild- and late-onset TAM and congenital miosis via constitutive activation of the CRAC channel. Our findings extend the clinical and genetic spectrum of the ORAI1-related TAM.


Assuntos
Mutação , Miopatias Congênitas Estruturais/genética , Proteína ORAI1/genética , Distúrbios Pupilares/congênito , Idade de Início , Canais de Cálcio Ativados pela Liberação de Cálcio/metabolismo , Feminino , Heterozigoto , Humanos , Masculino , Pessoa de Meia-Idade , Miopatias Congênitas Estruturais/fisiopatologia , Proteína ORAI1/metabolismo , Linhagem , Distúrbios Pupilares/genética
2.
Phys Rev Lett ; 111(26): 264801, 2013 Dec 27.
Artigo em Inglês | MEDLINE | ID: mdl-24483799

RESUMO

We review the theory of two color high gain free-electron laser emission, derive the integral equation characterizing the evolution of the optical intensities, and provide a description of the relevant dynamics. The characteristic feature of this regime is the existence of a mutual bunching, whose origin and role are discussed.

3.
Eur J Neurol ; 19(9): 1256-60, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22583668

RESUMO

BACKGROUND AND PURPOSE: Duchenne muscular dystrophy carriers represent a rare condition that needs to be recognized because of the possible implications for prenatal diagnosis. Muscle biopsy is currently the diagnostic instrument of choice in sporadic patients. We wanted to verify whether muscle magnetic resonance imaging (MRI) could identify a pattern of involvement suggestive of this condition and whether it was similar to that reported in Duchenne and Becker muscular dystrophy. METHODS: Evaluation of pelvic and lower limb MRI scans of 12 dystrophinopathy carriers was performed. RESULTS: We found a frequent involvement of the quadratus femoris, gluteus maximus and medius, biceps femoris long head, adductor magnus, vasti and paraspinal muscles, whilst the popliteus, iliopsoas, recti abdominis, sartorius, and gracilis were relatively spared. Asymmetry was a major feature on MRI; it could be detected significantly more often than with sole clinical examination and even in patients without weakness. CONCLUSIONS: The pattern we describe here is similar to that reported in Duchenne and Becker muscular dystrophy, although asymmetry represents a major distinctive feature. Muscle MRI was more sensitive than clinical examination for detecting single muscle involvement and asymmetry. Further studies are needed to verify the consistency of this pattern in larger cohorts and to assess whether muscle MRI can improve diagnostic accuracy in carriers with normal dystrophin staining on muscle biopsy.


Assuntos
Heterozigoto , Imageamento por Ressonância Magnética/métodos , Músculo Esquelético/patologia , Distrofia Muscular de Duchenne/patologia , Adulto , Doenças Assintomáticas , Estudos de Coortes , Feminino , Humanos , Extremidade Inferior/patologia , Pessoa de Meia-Idade , Distrofia Muscular de Duchenne/genética , Pelve/patologia , Estudos Retrospectivos
4.
J Theor Biol ; 256(3): 305-10, 2009 Feb 07.
Artigo em Inglês | MEDLINE | ID: mdl-18996401

RESUMO

Cancer growth dynamics, commonly simulated with a Gompertzian model, is analyzed in the framework of a more recent and realistic model. In particular, we consider the setting of a tumor embedded in a host organ and investigate their interaction. We assume that, at least in some cases, tumor metastasis may be triggered by an 'energetic crisis', when the tumor exceeds the 'carrying capacity' of the host organ. As a consequence, dissemination of clusters of cancer cells is set in motion, with a statistical probability given by a Poisson distribution. The model, although still at a preclinical level, is fully quantitative and is applied, as an example, to the case of prostate cancer. The results confirm that, at least for the more aggressive cancers, metastasis starts very early during tumorigenesis and a quantitative link is found between the tumor's doubling time, its 'aggressiveness' and the metastatic potential.


Assuntos
Modelos Estatísticos , Neoplasias/metabolismo , Neoplasias/patologia , Animais , Metabolismo Energético , Humanos , Masculino , Modelos Biológicos , Metástase Neoplásica , Probabilidade , Próstata/metabolismo , Neoplasias da Próstata/metabolismo , Neoplasias da Próstata/patologia , Fatores de Tempo
5.
J Mol Spectrosc ; 205(1): 173-176, 2001 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11148121

RESUMO

Formanilide has been investigated by free-jet millimeter-wave absorption spectroscopy. The rotational spectrum of the conformer with the formyl hydrogen anti to the phenyl group has been assigned. Several rotational transitions of the ground state have been measured for both normal and ND isotopic species. All the atoms of the peptidic group are coplanar to the ring. Copyright 2001 Academic Press.

6.
Minerva Med ; 73(32-33): 2091-100, 1982 Aug 25.
Artigo em Italiano | MEDLINE | ID: mdl-7099466

RESUMO

Recent and not so recent studies on acute poisoning by ethyl alcohol have confirmed that the substance acts directly on the nervous system both at cerebral cortex and subcortical formation level, and on the spinal cord, sense receptors and organs. The results of the various studies reveal the influence of drunkenness on pilots' capacity to fly a plane and on the relationship between this and plane crashes.


Assuntos
Medicina Aeroespacial , Intoxicação Alcoólica/complicações , Regulação da Temperatura Corporal/efeitos dos fármacos , Tronco Encefálico/efeitos dos fármacos , Permeabilidade da Membrana Celular/efeitos dos fármacos , Córtex Cerebral/efeitos dos fármacos , Etanol/efeitos adversos , Humanos , Hidrocortisona/metabolismo , Hipoglicemia/etiologia , Hipotálamo/efeitos dos fármacos , Junção Neuromuscular/efeitos dos fármacos , Pressorreceptores/efeitos dos fármacos , Medula Espinal/efeitos dos fármacos , Transtornos da Visão/etiologia
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