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authFullName_s : Claude Bendavid
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Maternal and neonatal outcomes and prognostic factors in acute fatty liver of pregnancy

Y. Joueidi , K. Peoc'H , Maela Le Lous , Guillaume Bouzille , Chloé Rousseau et al.
European Journal of Obstetrics & Gynecology and Reproductive Biology, 2020, 252, pp.198-205. ⟨10.1016/j.ejogrb.2020.06.052⟩
Journal articles hal-02931946v1

Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion.

Eilis A. Boudreau , Kyle P. Johnson , Angela R. Jackman , Jan Blancato , Marjan Huizing et al.
American Journal of Medical Genetics Part A, 2009, 149A (7), pp.1382-91. ⟨10.1002/ajmg.a.32846⟩
Journal articles inserm-00405710v1

Portable hemoglobinometer is a reliable technology for the follow-up of venesections tolerance in hemochromatosis.

Maxime Pawlowski , Fanny Latute , Edouard Bardou-Jacquet , Marianne Latournerie , Selim Zerrouki et al.
Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology, 2015, 39 (5), pp.570-575. ⟨10.1016/j.clinre.2014.09.014⟩
Journal articles hal-01134416v1
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Performance of a quick pregnancy test on whole blood in early pregnancy units a prospective cohort study

Caroline Legoupil , Isabelle Enderle , Flore-Anne Le Baccon , Claude Bendavid , Lucas Peltier et al.
European Journal of Emergency Medicine, 2019, 26 (2), pp.105-111. ⟨10.1097/MEJ.0000000000000501⟩
Journal articles hal-01808306v1

Twelve new patients with 13q deletion syndrome: Genotype-phenotype analyses in progress.

Chloé Quélin , Claude Bendavid , Christèle Dubourg , Céline de La Rochebrochard , Josette Lucas et al.
European Journal of Medical Genetics, 2009, 52 (1), pp.41-6. ⟨10.1016/j.ejmg.2008.10.002⟩
Journal articles istex inserm-00353241v1
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Gut bacteria are critical for optimal muscle functiona potential link with glucose homeostasis

Kevin Nay , Maxence Jollet , Benedicte Goustard , Narjes Baati , Barbara Vernus et al.
AJP - Endocrinology and Metabolism, 2019, 317 (1), pp.E158-E171. ⟨10.1152/ajpendo.00521.2018⟩
Journal articles hal-02152871v1

Pregnancy in metabolic diseases with hepatic expression what risks for the mother and the child?

Caroline Moreau , Yolaine Joueidi , Katell Peoc'H , Edouard Bardou-Jacquet , Maela Le Lous et al.
Annales de Biologie Clinique, 2019, 77 (6), pp.605-618. ⟨10.1684/abc.2019.1497⟩
Journal articles hal-02442524v1

Urinary TIMP-2 and MMP-2 are significantly associated with poor bladder compliance in adult patients with spina bifida

Benoit Peyronnet , Claire Richard , Claude Bendavid , Florian Naudet , Juliette Hascoet et al.
Neurourology and Urodynamics, 2019, 38 (8), pp.2151-2158. ⟨10.1002/nau.24163⟩
Journal articles hal-02304652v1
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Immunoassay Disruption by High-Dose Biotin Therapy: Fair Warning for Neonatal Care Physicians

Charles R Lefevre , Lucas Peltier , Léna Damaj , Jessica Valaize , Claude Bendavid et al.
Pediatric Neurology, 2020, 112, pp.8-9. ⟨10.1016/j.pediatrneurol.2020.07.007⟩
Journal articles hal-02930037v1
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Accuracy of citrulline, I-FABP and D-lactate in the diagnosis of acute mesenteric ischemia

Alexandre Nuzzo , Kevin Guedj , Sonja Curac , Claude Hercend , Claude Bendavid et al.
Scientific Reports, 2021, 11 (1), pp.18929. ⟨10.1038/s41598-021-98012-w⟩
Journal articles hal-03369677v1
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Beneficial effects of citrulline enteral administration on sepsis-induced T cell mitochondrial dysfunction

Florian Reizine , Murielle Grégoire , Mathieu Lesouhaitier , Valentin Coirier , Juliette Gauthier et al.
Proceedings of the National Academy of Sciences of the United States of America, 2022, 119 (8), pp.e2115139119. ⟨10.1073/pnas.2115139119⟩
Journal articles hal-03594344v1

The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.

Erich Roessler , Kenia B. El-Jaick , Christèle Dubourg , Jorge I. Vélez , Benjamin D. Solomon et al.
Human Mutation, 2009, 30 (10), pp.E921-35. ⟨10.1002/humu.21090⟩
Journal articles inserm-00406224v1

Metals common clinical applications in inductively coupled plasma mass spectrometry

Thibaud Cavey , Martine Ropert , Olivier Loréal , Claude Bendavid , Katell Peoc'H et al.
Annales de Biologie Clinique, 2019, 77 (5), pp.495-504. ⟨10.1684/abc.2019.1480⟩
Journal articles hal-02365038v1

Prévention des cancers du sein : de la chimioprévention à la chirurgie prophylactique [Breast cancer prevention: from chemoprevention to prophylactic surgery]

Karine Morcel , Sophie Rouquette , Catherine Dugast , Claude Bendavid , Odile Audrain et al.
Journal de Gynécologie Obstétrique et Biologie de la Reproduction, 2008, 37 (7), pp.661-71. ⟨10.1016/j.jgyn.2008.05.013⟩
Journal articles hal-00315848v1

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.

Sylvie Jaillard , Séverine Drunat , Claude Bendavid , Azzedine Aboura , Amandine Etcheverry et al.
European Journal of Medical Genetics, 2010, 53 (2), pp.66-75. ⟨10.1016/j.ejmg.2009.10.002⟩
Journal articles istex inserm-00434932v1

Elaboration of a new synovial predictive score of septic origin for acute arthritis on the native joint (RESAS)

Guillaume Coiffier , Olivia Berthoud , Jean David Albert , François Robin , Claire Goussault et al.
Rheumatology, 2021, 60 (5), pp.2238-2245. ⟨10.1093/rheumatology/keaa567⟩
Journal articles hal-03038273v1

Illustrations cliniques d’un manque de cardiospécificité du dosage de troponine T hypersensible

Valentin Coirier , Romain Pelletier , Martine Sébillot , Charles R Lefèvre , Lucas Peltier et al.
Annales de Biologie Clinique, 2021, 79 (2), pp.176-180. ⟨10.1684/abc.2021.1637⟩
Journal articles hal-03223963v1


Mathieu Lesouhaitier , Fabrice Uhel , Murielle Grégoire , Arnaud Gacouin , Aurelien Frerou et al.
Shock, 2022, 58 (6), pp.476-483. ⟨10.1097/SHK.0000000000002007⟩
Journal articles hal-03967873v1
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New insights into the genetic basis of premature ovarian insufficiency: Novel causative variants and candidate genes revealed by genomic sequencing

Sylvie Jaillard , K.W. Bell , Linda Akloul , K Walton , Kenneth Mcelreavy et al.
Maturitas, 2020, 141, pp.9-19. ⟨10.1016/j.maturitas.2020.06.004⟩
Journal articles hal-02931925v1

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.

Erich Roessler , Yong Ma , Maia Ouspenskaia , Felicitas Lacbawan , Claude Bendavid et al.
Human Genetics, 2009, 125 (4), pp.393-400. ⟨10.1007/s00439-009-0628-7⟩
Journal articles inserm-00366120v1

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).

Sandra Mercier , Christèle Dubourg , Marion Belleguic , Laurent Pasquier , Philippe Loget et al.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2010, 154C (1), pp.191-6. ⟨10.1002/ajmg.c.30246⟩
Journal articles istex inserm-00461987v1
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Holoprosencephaly: An update on cytogenetic abnormalities.

Claude Bendavid , Valérie Dupé , Lucie Rochard , Isabelle Gicquel , Christèle Dubourg et al.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2010, 154C (1), pp.86-92. ⟨10.1002/ajmg.c.30250⟩
Journal articles inserm-00462057v1
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New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Sandra Mercier , Christèle Dubourg , Nicolas Garcelon , Boris Campillo-Gimenez , Isabelle Gicquel et al.
Journal of Medical Genetics, 2011, 48 (11), pp.752-60. ⟨10.1136/jmedgenet-2011-100339⟩
Journal articles inserm-00626407v1
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Performance of a new rapid diagnostic test the lactate/glucose ratio of synovial fluid for the diagnosis of septic arthritis

Pascal Guggenbuhl , Olivia Berthoud , Guillaume Coiffier , Jean-David Albert , Anne Gougeon-Jolivet et al.
Joint Bone Spine, 2020, 87 (4), pp.343-350. ⟨10.1016/j.jbspin.2020.03.009⟩
Journal articles hal-02563465v1
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Caesarean section at term: the relationship between neonatal respiratory morbidity and microviscosity in amniotic fluid.

Vincent Lavoué , Laure Voguet , Bruno Laviolle , Caroline Piau , Marie Pascale Beaumont et al.
European Journal of Obstetrics & Gynecology and Reproductive Biology, 2013, 169 (2), pp.239-43. ⟨10.1016/j.ejogrb.2013.05.003⟩
Journal articles hal-00860266v1
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Spleen iron, molybdenum, and manganese concentrations are coregulated in hepcidin-deficient and secondary iron overload models in mice

Thibault Cavey , Chloé Latour , Marie-Laure Island , Patricia Leroyer , Pascal Guggenbuhl et al.
FASEB Journal, 2019, 33 (10), pp.11072-11081. ⟨10.1096/fj.201801381RR⟩
Journal articles hal-02281402v1
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Mouse genetic background impacts both on iron and non-iron metals parameters and on their relationships

Thibault Cavey , Martine Ropert , Marie De Tayrac , Edouard Bardou-Jacquet , Marie-Laure Island et al.
BioMetals, 2015, 28 (4), pp.733-743. ⟨10.1007/s10534-015-9862-8⟩
Journal articles hal-01162386v1
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Evaluation of the Impact of Renal Failure on Correlation and Concordance Between 2 Free Light Chain Assays

Caroline Moreau , Brice Autier , Thibault Cavey , Emmanuel Rouger , James Norwood et al.
Clinical lymphoma, 2016, 16 (12), pp.693-704. ⟨10.1016/j.clml.2016.08.012⟩
Journal articles hal-01427008v1
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Infrared photoelectrochemical sensing of urea with silicon photoanodes

Joudi Dabboussi , Y. Zhao , R. Abdallah , A. Gicquel , Claude Bendavid et al.
Biosensors and Bioelectronics: X, 2022, 12, pp.100221. ⟨10.1016/j.biosx.2022.100221⟩
Journal articles hal-03798873v1
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Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Karine Morcel , Tanguy Watrin , Laurent Pasquier , Lucie Rochard , Cédric Le Caignec et al.
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.9. ⟨10.1186/1750-1172-6-9⟩
Journal articles inserm-00582863v1