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1.
Clin Genet ; 91(5): 780-786, 2017 May.
Article in English | MEDLINE | ID: mdl-27882542

ABSTRACT

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.


Subject(s)
Mutation , Myopathies, Structural, Congenital/genetics , ORAI1 Protein/genetics , Pupil Disorders/congenital , Age of Onset , Calcium Release Activated Calcium Channels/metabolism , Female , Heterozygote , Humans , Male , Middle Aged , Myopathies, Structural, Congenital/physiopathology , ORAI1 Protein/metabolism , Pedigree , Pupil Disorders/genetics
2.
Phys Rev Lett ; 111(26): 264801, 2013 Dec 27.
Article in English | MEDLINE | ID: mdl-24483799

ABSTRACT

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.
Article in English | MEDLINE | ID: mdl-22583668

ABSTRACT

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.


Subject(s)
Heterozygote , Magnetic Resonance Imaging/methods , Muscle, Skeletal/pathology , Muscular Dystrophy, Duchenne/pathology , Adult , Asymptomatic Diseases , Cohort Studies , Female , Humans , Lower Extremity/pathology , Middle Aged , Muscular Dystrophy, Duchenne/genetics , Pelvis/pathology , Retrospective Studies
4.
J Theor Biol ; 256(3): 305-10, 2009 Feb 07.
Article in English | MEDLINE | ID: mdl-18996401

ABSTRACT

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.


Subject(s)
Models, Statistical , Neoplasms/metabolism , Neoplasms/pathology , Animals , Energy Metabolism , Humans , Male , Models, Biological , Neoplasm Metastasis , Probability , Prostate/metabolism , Prostatic Neoplasms/metabolism , Prostatic Neoplasms/pathology , Time Factors
5.
J Mol Spectrosc ; 205(1): 173-176, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11148121

ABSTRACT

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.
Article in Italian | MEDLINE | ID: mdl-7099466

ABSTRACT

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.


Subject(s)
Aerospace Medicine , Alcoholic Intoxication/complications , Body Temperature Regulation/drug effects , Brain Stem/drug effects , Cell Membrane Permeability/drug effects , Cerebral Cortex/drug effects , Ethanol/adverse effects , Humans , Hydrocortisone/metabolism , Hypoglycemia/etiology , Hypothalamus/drug effects , Neuromuscular Junction/drug effects , Pressoreceptors/drug effects , Spinal Cord/drug effects , Vision Disorders/etiology
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