Search Results - "Roth, P. M"
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1
Shift in skin microbiota of Western European women across aging
Published in Journal of applied microbiology (01-09-2018)“…Aims The objective of our study was to compare the microbiota diversity between two different age groups of Western European women. Methods and Results…”
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2
Hough-based tracking of non-rigid objects
Published in Computer vision and image understanding (01-10-2013)“…► We track previously unknown non-rigid objects by learning their appearance. ► A rough segmentation avoids the bounding-box restriction of previous…”
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3
Bone status in a mouse model of genetic hemochromatosis
Published in Osteoporosis international (01-08-2011)“…Summary Genetic hemochromatosis is a cause of osteoporosis; mechanisms leading to iron-related bone loss are not fully characterized. We assessed the bone…”
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4
Associated malformations in patients with anorectal anomalies
Published in European journal of medical genetics (01-07-2007)“…Abstract Patients with congenital anorectal malformations (ARM) often have other associated congenital defects. The reported incidence and the types of…”
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5
Acid reflux event detection using the Bravo wireless versus the Slimline catheter pH systems: why are the numbers so different?
Published in Gut (01-12-2005)“…Objective: This study analysed the relative accuracy of the Bravo wireless and the Slimline catheter-Mark III Digitrapper pH systems in the detection of acid…”
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6
Duodenal mRNA expression of iron related genes in response to iron loading and iron deficiency in four strains of mice
Published in Gut (01-11-2002)“…Background: Although much progress has been made recently in characterising the proteins involved in duodenal iron trafficking, regulation of intestinal iron…”
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7
Associated anomalies in Pierre Robin sequence
Published in American journal of medical genetics. Part A (01-09-2023)“…Pierre Robin sequence (PRS) is frequently co‐occurring with other non‐PRS congenital anomalies. The types and the prevalence of anomalies co‐occurring with PRS…”
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8
Associated malformations in cases with congenital diaphragmatic hernia
Published in Genetic counseling (01-01-2008)“…The etiology of congenital diaphragmatic hernia (CDH) is unclear and its pathogenesis is controversial. Because previous reports have inconsistently noted the…”
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9
Associated malformations in cases with oral clefts
Published in The Cleft palate-craniofacial journal (2000)“…Infants with oral clefts (OCs) often have other associated congenital defects. The reported incidence and the types of associated malformations vary between…”
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10
Stress Chatter via Fluid Flow and Fault Slip in a Hydraulic Fracturing‐Induced Earthquake Sequence in the Montney Formation, British Columbia
Published in Geophysical research letters (28-07-2020)“…Source processes of injection‐induced earthquakes involve complex fluid‐rock interaction often elusive to regional seismic monitoring. Here we combine…”
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ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA
Published in Genetic counseling (01-01-2015)“…Cases with congenital diaphragmatic hernia (CDH) often have other associated anomalies. The purpose of this investigation was to assess the prevalence and the…”
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12
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews
Published in Gut (01-04-1993)“…The Jewish population has an increased frequency of inflammatory bowel disease compared with their non-Jewish neighbours. Genetic factors have been implicated…”
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13
Associated malformations among infants with radial ray deficiency
Published in Genetic counseling (01-01-2013)“…Infants with radial ray deficiencies very often have other associated congenital anomalies. The reported frequency and types of associated malformations vary…”
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14
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians
Published in BMJ (19-07-2003)“…Finding people over 99 years old who are homozygous for the C282Y mutation and still alive without treatment confirms that clinical penetrance in homozygotes…”
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15
Identification of a new locus for isolated familial keratoconus at 2p24
Published in Journal of medical genetics (01-01-2005)“…Histological observations have demonstrated degradation of the corneal epithelium basal membrane, diminution of the number of collagen fibrils, thinning of the…”
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16
Comparison of esophageal acid exposure at 1 cm and 6 cm above the squamocolumnar junction using the Bravo™ pH monitoring system
Published in Diseases of the esophagus (01-06-2006)“…The aim of this study was to assess the quantitative differences of acid exposure at 1 cm and 6 cm above the squamocolumnar junciton (SCJ) using two…”
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17
From the morphological to the transcriptomic characterization of a compromised three-dimensional in vitro model mimicking atopic dermatitis
Published in British journal of dermatology (1951) (01-10-2015)“…Summary Background Atopic dermatitis (AD) is a chronic inflammatory skin disease in which skin barrier function is disrupted. In this AD environment,…”
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18
Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex
Published in Genomics (San Diego, Calif.) (15-07-1997)“…Analysis of 784 informative meioses in the CEPH pedigrees revealed a total of 22 recombination events having occurred in the 6-Mb region between D6S265 (70 kb…”
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19
Source Properties of Hydraulic‐Fracturing‐Induced Earthquakes in the Kiskatinaw Area, British Columbia, Canada
Published in Journal of geophysical research. Solid earth (01-03-2022)“…This work presents a high resolution source property study of hydraulic fracturing induced earthquakes in the Montney Formation, a low‐permeability tight shale…”
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20
A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the rat
Published in Genes and immunity (01-01-2004)“…Multiple sclerosis (MS) is a chronic immune-mediated demyelinating disease of the central nervous system. Evidence from family studies indicates a strong…”
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