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1.
J Neurol Neurosurg Psychiatry ; 92(5): 479-484, 2021 05.
Article in English | MEDLINE | ID: mdl-33408239

ABSTRACT

OBJECTIVES: To determine whether the familial clustering of amyotrophic lateral sclerosis (ALS) cases and the phenotype of the disease may help identify the pathogenic genes involved. METHODS: We conducted a targeted next-generation sequencing analysis on 235 French familial ALS (FALS), unrelated probands to identify mutations in 30 genes linked to the disease. The genealogy, that is, number of cases and generations with ALS, gender, age, site of onset and the duration of the disease were analysed. RESULTS: Regarding the number of generations, 49 pedigrees had only one affected generation, 152 had two affected generations and 34 had at least three affected generations. Among the 149 pedigrees (63.4%) for which a deleterious variant was found, an abnormal G4C2 expansion in C9orf72 was found in 98 cases as well as SOD1, TARBP or FUS mutations in 30, 9 and 7 cases, respectively. Considering pedigrees from the number of generations, abnormal G4C2 expansion in C9orf72 was more frequent in pedigrees with pairs of affected ALS cases, which represented 65.2% of our cohort. SOD1 mutation involved all types of pedigrees. No TARDBP nor FUS mutation was present in monogenerational pedigrees. TARDBP mutation predominated in bigenerational pedigrees with at least three cases and FUS mutation in multigenerational pedigrees with more than seven cases, on average, and with an age of onset younger than 45 years. CONCLUSION: Our results suggest that familial clustering, phenotypes and genotypes are interconnected in FALS, and thus it might be possible to target the genetic screening from the familial architecture and the phenotype of ALS cases.


Subject(s)
Amyotrophic Lateral Sclerosis/genetics , C9orf72 Protein/genetics , Mutation , Aged , Cluster Analysis , DNA Mutational Analysis , DNA-Binding Proteins/genetics , Female , Genetic Testing , Genotype , High-Throughput Nucleotide Sequencing , Humans , Male , Middle Aged , Pedigree , Phenotype , RNA-Binding Protein FUS/genetics , Superoxide Dismutase-1/genetics
2.
ACS Appl Mater Interfaces ; 6(3): 1893-901, 2014 Feb 12.
Article in English | MEDLINE | ID: mdl-24428348

ABSTRACT

Atomic layer deposition (ALD) is a thin film deposition technique that is based on alternating and saturating surface reactions of two or more gaseous precursors. The excellent conformality of ALD thin films can be exploited for sealing defects in coatings made by other techniques. Here the corrosion protection properties of hard CrN and diamond-like carbon (DLC) coatings on low alloy steel were improved by ALD sealing with 50 nm thick layers consisting of Al2O3 and Ta2O5 nanolaminates or mixtures. In cross sectional images the ALD layers were found to follow the surface morphology of the CrN coatings uniformly. Furthermore, ALD growth into the pinholes of the CrN coating was verified. In electrochemical measurements the ALD sealing was found to decrease the current density of the CrN coated steel by over 2 orders of magnitude. The neutral salt spray (NSS) durability was also improved: on the best samples the appearance of corrosion spots was delayed from 2 to 168 h. On DLC coatings the adhesion of the ALD sealing layers was weaker, but still clear improvement in NSS durability was achieved indicating sealing of the pinholes.

3.
J Neurol ; 259(6): 1222-6, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22179783

ABSTRACT

Tangier disease (TD) (OMIM#205400) is a rare autosomal recessive disorder resulting from mutations in the ABCA1 gene, leading to decreased levels of plasma high-density lipoproteins (HDL). Peripheral neuropathy is a common finding in this disease, and may present as relapsing/remitting mono/polyneuropathies or as syringomyelia-like neuropathy. We retrospectively analyzed four patients, and report here their clinical, biological, electrophysiological, imaging, and genetic findings. Three patients had a typical pseudosyringomyelic neuropathy including facial diplegia, but asymmetrical onset was observed in one patient who had first been misdiagnosed with Lewis-Sumner syndrome. Electrophysiological pattern was heterogeneous, showing both signs of demyelination and axonal degeneration. Truncating mutations of the ABCA1 gene, including two previously undescribed mutations, were constantly found. Atypical symptom onset and demyelinating features on electrophysiological examination can be misleading in case of pseudosyringomyelic neuropathy. These reports illustrate two different neurological phenotypes in TD, namely the pseudosyringomyelic type and the Lewis-Sumner-like type, and advocate for a systematic assessment of lipid profile including HDL cholesterol in demyelinating neuropathies.


Subject(s)
Peripheral Nervous System Diseases/diagnosis , Peripheral Nervous System Diseases/physiopathology , Tangier Disease/diagnosis , ATP Binding Cassette Transporter 1 , ATP-Binding Cassette Transporters/genetics , Adult , Electrophysiological Phenomena/physiology , Humans , Male , Middle Aged , Peripheral Nervous System Diseases/complications , Retrospective Studies , Tangier Disease/complications , Tangier Disease/physiopathology
4.
J Neurol Sci ; 291(1-2): 100-2, 2010 Apr 15.
Article in English | MEDLINE | ID: mdl-20117795

ABSTRACT

A 60-year-old woman presented with a 1-week progressive limb weakness and an areflexic tetraparesis. Both neurophysiological and cerebrospinal fluid examinations were consistent with diagnosis of Guillain-Barré syndrome (GBS) and a treatment by intravenous immunoglobulin over a 5-day period was started. At the end of the treatment, the patient suffered from an acute coronary syndrome (ACS) without stenosis at coronary arteriography. Left ventriculography showed segmental wall motion abnormalities with apical akinesis contrasting with hyperkinesis in basal segments, with a depressed left ventricular ejection fraction at 45%. Cardiac magnetic resonance imaging excluded the diagnosis of myocarditis. A diagnosis of "transient left ventricular apical ballooning syndrome" or "Takotsubo" syndrome was then made and a treatment by angiotensin-converting enzyme inhibitor and beta-blocker was introduced. Left ventricular dysfunction and electrocardiogram normalized within two weeks and the patient remained free from cardiovascular events at one year of follow-up. This cardiomyopathy is a recently known and now commonly diagnosed reversible systolic dysfunction mimicking ACS and is secondary to physical or emotional stress affecting mainly post-menopausal women. Electrocardiographic and echocardiographic abnormalities are often regressive in days or weeks, and rarely responsible for complications. This observation supports clinical evidence that electrocardiographic changes in GBS can be linked to Takotsubo syndrome, by means of the stressful trigger of GBS occurrence. This reversible cardiomyopathy needs adequate management and specific therapeutic strategies. Therefore, trans-thoracic echocardiography should be systematically performed when repolarisation abnormalities are present in this disease to rule out a Takotsubo syndrome, even in asymptomatic patients.


Subject(s)
Guillain-Barre Syndrome/diagnosis , Takotsubo Cardiomyopathy/diagnosis , Diagnosis, Differential , Electrocardiography , Female , Follow-Up Studies , Guillain-Barre Syndrome/complications , Guillain-Barre Syndrome/drug therapy , Heart/physiopathology , Humans , Magnetic Resonance Imaging , Middle Aged , Myocardium/pathology , Primary Dysautonomias/diagnosis , Primary Dysautonomias/pathology , Takotsubo Cardiomyopathy/complications , Takotsubo Cardiomyopathy/drug therapy , Treatment Outcome
5.
J Neurol ; 257(5): 792-8, 2010 May.
Article in English | MEDLINE | ID: mdl-20012543

ABSTRACT

The aetiology of sporadic ALS is still unknown. Links with several environmental factors have been suggested, and some epidemiological studies have shown an increased incidence of ALS in rural populations. This study was designed to investigate risk exposures in a well-delimited rural population and to assess whether rural residency or occupations, such as farming, were associated with an increased risk of developing ALS. A prospective case-control-study of 108 sporadic ALS cases matched by age and sex to 122 controls was performed in Brittany from 2006 to 2008. A strong association was found between agricultural activity and ALS (odds ratio: 2.919; p = 0.01), while rural residence itself did not influence the risk of the disease. Bulbar forms of onset prevailed among agricultural workers as compared with other occupations (55 vs. 26%; p = 0.009). These results suggest a potential role of exposure to agricultural chemicals or contact with animals linked to agricultural work. The prevalence of bulbar forms of onset in agricultural workers has not been reported before. In addition to variable methodological approaches, differences in agricultural practices could explain the discrepancy between these findings and other studies.


Subject(s)
Amyotrophic Lateral Sclerosis/epidemiology , Environmental Exposure , Rural Population , Adult , Aged , Aged, 80 and over , Agriculture , Case-Control Studies , Female , France , Humans , Male , Middle Aged , Occupational Exposure , Prevalence , Risk Factors
6.
Phys Rev E Stat Nonlin Soft Matter Phys ; 72(5 Pt 2): 056402, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16383761

ABSTRACT

In dc magnetrons the electrons emitted from the cathode may return there due to the applied magnetic field. When that happens, they can be recaptured or reflected back into the discharge, depending on the value of the reflection coefficient (RC). A 2d3v (two-dimensional in coordinate and three-dimensional in velocity space) particle-in-cell-Monte Carlo model, including an external circuit, is developed to determine the role of the electron recapture in the discharge processes. The detailed discharge structure as a function of RC for two pressures (4 and 25 mtorr) is studied. The importance of electron recapture is clearly manifested, especially at low pressures. The results indicate that the discharge characteristics are dramatically changed with varying RC between 0 and 1. Thus, the electron recapture at the cathode appears to be a significant mechanism in magnetron discharges and RC a very important parameter in their correct quantitative description that should be dealt with cautiously.

7.
J Environ Monit ; 6(10): 834-40, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15480498

ABSTRACT

The paper presents a lidar study of the aerosol structure in the planetary boundary layer in the case of radiation fog and haze. A conceptual model of the dynamics of the depolarization coefficient profile during the mixing layer development, taking into account the presence of a multilayered inversions and radiation fogs, is proposed. Various techniques are employed in the processing of the lidar signal in order to determine the mixing layer height as well as more details of the aerosol structure in the low atmosphere, namely, finding the maximum of the signal returned from the lowest temperature inversion, the crossing point of the S function's first derivative with the x axis, and profiles of the depolarization ratio. After the complete destruction of the stable stratification, a low constant value of the depolarization ratio within the newly formed mixing layer is being observed. The study of stable boundary layer disintegration and convective boundary layer formation in the presence of fogs and/or clouds is of both scientific and practical significance in what concerns the protection of the environment and the aviation meteorology.


Subject(s)
Atmosphere/analysis , Environmental Monitoring/methods , Meteorological Concepts , Air Movements , Altitude , Bulgaria , Cities , Humidity , Lasers , Models, Theoretical , Radiation
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