Arama Sonuçları - Élise Schaefer
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 34
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1
Porn Studies Yazar: Rich Cante, Constance Pen- Ley, Angelo Restivo, Élise Schaefer
Baskı/Yayın Bilgisi 2004Livro -
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Breastfeeding Outcome Comparison by Parity Yazar: Nicole M. Hackman, Élise Schaefer, Jessica S. Beiler, Chelsea M. Rose, Ian M. Paul
Baskı/Yayın Bilgisi 2014Artigo -
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National Survey of School Employees: <scp>COVID</scp>‐19, School Reopening, and Student Wellness Yazar: Krista L. Pattison, Alicia M. Hoke, Élise Schaefer, Jeanie Alter, Deepa L. Sekhar
Baskı/Yayın Bilgisi 2021Artigo -
6
Positive and Negative Volume-Outcome Relationships in the Geriatric Trauma Population Yazar: Kazuhide Matsushima, Élise Schaefer, Eugene Won, Scott B. Armen, Matthew Indeck, David I. Soybel
Baskı/Yayın Bilgisi 2014Artigo -
7
Early Weight Loss Nomograms for Exclusively Breastfed Newborns Yazar: Valerie J. Flaherman, Élise Schaefer, Michael W. Kuzniewicz, Sherian X. Li, Eileen M. Walsh, Ian M. Paul
Baskı/Yayın Bilgisi 2014Artigo -
8
New perspectives on community-acquired pneumonia in 388 406 patients. Results from a nationwide mandatory performance measurement programme in healthcare quality Yazar: Santiago Ewig, Norbert Birkner, Richard Strauß, Élise Schaefer, J Pauletzki, Helge Bischoff, Paul Schraeder, Tobias Welte, Gert Hoeffken
Baskı/Yayın Bilgisi 2009Artigo -
9
Association of Preoperative Anti–Tumor Necrosis Factor Therapy With Adverse Postoperative Outcomes in Patients Undergoing Abdominal Surgery for Ulcerative Colitis Yazar: Audrey S. Kulaylat, Afif N. Kulaylat, Élise Schaefer, Andrew Tinsley, Emmanuelle Williams, Walter A. Koltun, Christopher S. Hollenbeak, Evangelos Messaris
Baskı/Yayın Bilgisi 2017Artigo -
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Should Large Cell Neuroendocrine Lung Carcinoma be Classified and Treated as a Small Cell Lung Cancer or with Other Large Cell Carcinomas? Yazar: John M. Varlotto, Laura N. Medford‐Davis, Abram Recht, John C. Flíckinger, Élise Schaefer, Dani S. Zander, Malcolm M. DeCamp
Baskı/Yayın Bilgisi 2011Artigo -
12
Screening in High Schools to Identify, Evaluate, and Lower Depression Among Adolescents Yazar: Deepa L. Sekhar, Élise Schaefer, James G. Waxmonsky, Leslie R. Walker-Harding, Krista L. Pattison, Alissa Molinari, Perri Rosen, Jennifer L. Kraschnewski
Baskı/Yayın Bilgisi 2021Artigo -
13
A phase 2 study of vorinostat in acute myeloid leukemia Yazar: Élise Schaefer, Arturo Loaiza‐Bonilla, Mark Juckett, John F. DiPersio, Vivek Roy, James L. Slack, Wenting Wu, K. M. Laumann, Igor Espinoza‐Delgado, S. D. Gore
Baskı/Yayın Bilgisi 2009Artigo -
14
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome Yazar: Élise Schaefer, Corinne Collet, David Geneviève, Marie Vincent, Dietmar Lohmann, Elodie Sanchez, Chantal Bolender, Marie‐Madeleine Eliot, Gudrun Nürnberg, Maria-Rita Passos-Bueno, Dagmar Wieczorek, Lionel Van Maldergem, Bérénice Doray
Baskı/Yayın Bilgisi 2014Artigo -
15
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal Genes Yazar: Corinne Collet, Agnès Ostertag, Manon Ricquebourg, Marine Delecourt, Giulia Tueur, Bertrand Isidor, Pascale V. Guillot, Élise Schaefer, Rose‐Marie Javier, Thomas Funck‐Brentano, Philippe Orcel, Jean Laplanche, Martine Cohen‐Solal
Baskı/Yayın Bilgisi 2017Artigo -
16
Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit<i>BBIP1</i>(<i>BBS18</i>) Yazar: Sophie Scheidecker, Christelle Etard, Nathan W. Pierce, Véronique Geoffroy, Élise Schaefer, Jean Muller, Kirsley Chennen, Elisabeth Flori, Valérie Pelletier, Olivier Poch, Vincent Marion, Corinne Stoetzel, Uwe Strähle, Maxence V. Nachury, Hélène Dollfus
Baskı/Yayın Bilgisi 2013Artigo -
17
Mutations in Histone Acetylase Modifier BRPF1 Cause an Autosomal-Dominant Form of Intellectual Disability with Associated Ptosis Yazar: Francesca Mattioli, Élise Schaefer, Alex Magee, Paul R. Mark, Grazia M.S. Mancini, Klaus Dieterich, Gretchen Von Allmen, Mariëlle Alders, Charles Coutton, Marjon van Slegtenhorst, Gaëlle Vieville, Marc Engelen, Jan Maarten Cobben, Jane Juusola, Aurora Pujol, Jean‐Louis Mandel, Amélie Piton
Baskı/Yayın Bilgisi 2016Artigo -
18
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly Yazar: Élise Schaefer, Ariane Zaloszyc, Julia Lauer, M. Durand, Fanny Stutzmann, Y. Perdomo-Trujillo, Claire Redin, V. Bennouna Greene, Annick Toutain, Laurence Perrin, Marion Gérard, Sophie Caillard, Xiaoshu Bei, Richard A. Lewis, D Christmann, J. Letsch, M. Kribs, Catherine Schmidt‐Mutter, Jean Muller, Corinne Stoetzel, Michel Fischbach, Vincent Marion, Nicholas Katsanis, Hélène Dollfus
Baskı/Yayın Bilgisi 2010Artigo -
19
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract Yazar: Laurence Heidet, Vincent Morinière, C. Henry, Lara De Tomasi, Madeline Louise Reilly, Camille Humbert, Olivier Alibeu, Cécile Fourrage, Christine Bôle‐Feysot, Patrick Nitschké, Frédéric Torès, Marc Bras, Marc Jeanpierre, Christine Piétrement, Dominique Gaillard, Marie Gonzalès, Robert Novo, Élise Schaefer, J. Roume, Jéléna Martinovic, Valérie Malan, Rémi Salomon, Sophie Saunier, Corinne Antignac, Marc Jeanpierre
Baskı/Yayın Bilgisi 2017Artigo -
20
Proteasome subunit <i>PSMC3</i> variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress Yazar: Ariane Kröll‐Hermi, Frédéric Ebstein, Corinne Stoetzel, Véronique Geoffroy, Élise Schaefer, Sophie Scheidecker, Séverine Bär, Masanari Takamiya, Koichi Kawakami, Barbara A. Zieba, Fouzia Studer, Valérie Pelletier, C. Eyermann, Claude Speeg‐Schatz, Vincent Laugel, Dan Lipsker, Florian Sandron, Steven McGinn, Anne Boland, Jean‐François Deleuze, Lauriane Kühn, Johana Chicher, Philippe Hammann, Sylvie Friant, Christelle Etard, Elke Krüger, Jean Muller, Uwe Strähle, Hélène Dollfus
Baskı/Yayın Bilgisi 2020Artigo
Arama Araçları:
İlgili Konular
Biology
Genetics
Medicine
Gene
Internal medicine
Phenotype
Mutation
Pediatrics
Surgery
Bioinformatics
Computational biology
Disease
Exome sequencing
Microcephaly
Neuroscience
Pathology
Psychiatry
Psychology
Genotype
Intellectual disability
Missense mutation
Obstetrics
Physics
Pregnancy
Protein subunit
Anatomy
Anxiety
Bardet–Biedl syndrome
Breastfeeding
Candidate gene