Results
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541.
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Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome. [electronic resource] by
- Lemire, Gabrielle T
- Beauregard-Lacroix, Éliane
- Campeau, Philippe M
- Parent, Stefan
- Roy-Beaudry, Marjolaine
- Soglio, Dorothée Dal
- Grignon, Andrée
- Rypens, Françoise
- Wavrant, Sandrine
- Laberge, Anne-Marie
- Delrue, Marie-Ange
Producer: 20210203
In:
American journal of medical genetics. Part A vol. 182
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542.
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Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome. [electronic resource] by
- Bélanger, Catherine
- Bérubé-Simard, Félix-Antoine
- Leduc, Elizabeth
- Bernas, Guillaume
- Campeau, Philippe M
- Lalani, Seema R
- Martin, Donna M
- Bielas, Stephanie
- Moccia, Amanda
- Srivastava, Anshika
- Silversides, David W
- Pilon, Nicolas
Producer: 20180718
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 115
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543.
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Bioactive phloroglucinols from Mallotus oppositifolius. [electronic resource] by
- Kabran, Faustin A
- Okpekon, Timothée A
- Roblot, François
- Séon-Méniel, Blandine
- Leblanc, Karine
- Bories, Christian
- Champy, Pierre
- Yolou, Séri F
- Loiseau, Philippe M
- Djakouré, Léon A
- Figadère, Bruno
- Maciuk, Alexandre
Producer: 20160412
In:
Fitoterapia vol. 107
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544.
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Control of intestinal homeostasis, colitis, and colitis-associated colorectal cancer by the inflammatory caspases. [electronic resource] by
- Dupaul-Chicoine, Jeremy
- Yeretssian, Garabet
- Doiron, Karine
- Bergstrom, Kirk S B
- McIntire, Christian R
- LeBlanc, Philippe M
- Meunier, Charles
- Turbide, Claire
- Gros, Philippe
- Beauchemin, Nicole
- Vallance, Bruce A
- Saleh, Maya
Producer: 20100421
In:
Immunity vol. 32
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545.
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Adult presentation of X-linked Conradi-Hünermann-Happle syndrome. [electronic resource] by
- Posey, Jennifer E
- Burrage, Lindsay C
- Campeau, Philippe M
- Lu, James T
- Eble, Tanya N
- Kratz, Lisa
- Schlesinger, Alan E
- Gibbs, Richard A
- Lee, Brendan H
- Nagamani, Sandesh C S
Producer: 20160219
In:
American journal of medical genetics. Part A vol. 167
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546.
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Efficacy of orally administered 2-substituted quinolines in experimental murine cutaneous and visceral leishmaniases. [electronic resource] by
- Nakayama, Hector
- Loiseau, Philippe M
- Bories, Christian
- Torres de Ortiz, Susana
- Schinini, Alicia
- Serna, Elsa
- Rojas de Arias, Antonieta
- Fakhfakh, Mohamed A
- Franck, Xavier
- Figadère, Bruno
- Hocquemiller, Reynald
- Fournet, Alain
Producer: 20060314
In:
Antimicrobial agents and chemotherapy vol. 49
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547.
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Pneumocystis jirovecii pneumonia: still a concern in patients with haematological malignancies and stem cell transplant recipients. [electronic resource] by
- Cordonnier, Catherine
- Cesaro, Simone
- Maschmeyer, Georg
- Einsele, Hermann
- Donnelly, J Peter
- Alanio, Alexandre
- Hauser, Philippe M
- Lagrou, Katrien
- Melchers, Willem J G
- Helweg-Larsen, Jannik
- Matos, Olga
- Bretagne, Stéphane
- Maertens, Johan
Producer: 20170815
In:
The Journal of antimicrobial chemotherapy vol. 71
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548.
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ECIL guidelines for the diagnosis of Pneumocystis jirovecii pneumonia in patients with haematological malignancies and stem cell transplant recipients. [electronic resource] by
- Alanio, Alexandre
- Hauser, Philippe M
- Lagrou, Katrien
- Melchers, Willem J G
- Helweg-Larsen, Jannik
- Matos, Olga
- Cesaro, Simone
- Maschmeyer, Georg
- Einsele, Hermann
- Donnelly, J Peter
- Cordonnier, Catherine
- Maertens, Johan
- Bretagne, Stéphane
Producer: 20170815
In:
The Journal of antimicrobial chemotherapy vol. 71
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549.
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ECIL guidelines for preventing Pneumocystis jirovecii pneumonia in patients with haematological malignancies and stem cell transplant recipients. [electronic resource] by
- Maertens, Johan
- Cesaro, Simone
- Maschmeyer, Georg
- Einsele, Hermann
- Donnelly, J Peter
- Alanio, Alexandre
- Hauser, Philippe M
- Lagrou, Katrien
- Melchers, Willem J G
- Helweg-Larsen, Jannik
- Matos, Olga
- Bretagne, Stéphane
- Cordonnier, Catherine
Producer: 20170815
In:
The Journal of antimicrobial chemotherapy vol. 71
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550.
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Pneumocystis jirovecii pneumonia: still a concern in patients with haematological malignancies and stem cell transplant recipients-authors' response. [electronic resource] by
- Cordonnier, Catherine
- Alanio, Alexandre
- Cesaro, Simone
- Maschmeyer, Georg
- Einsele, Hermann
- Donnelly, J Peter
- Hauser, Philippe M
- Lagrou, Katrien
- Melchers, Willem J G
- Helweg-Larsen, Jannik
- Matos, Olga
- Bretagne, Stéphane
- Maertens, Johan
Producer: 20180130
In:
The Journal of antimicrobial chemotherapy vol. 72
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551.
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Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7). [electronic resource] by
- Whyte, Michael P
- Campeau, Philippe M
- McAlister, William H
- Roodman, G David
- Kurihara, Nori
- Nenninger, Angela
- Duan, Shenghui
- Gottesman, Gary S
- Bijanki, Vinieth N
- Sedighi, Homer
- Veis, Deborah J
- Mumm, Steven
Producer: 20210617
In:
Bone vol. 137
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552.
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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates. [electronic resource] by
- Eckl, Katja Martina
- Stevens, Howard P
- Lestringant, Gilles G
- Westenberger-Treumann, Margaretha
- Traupe, Heiko
- Hinz, Britta
- Frossard, Philippe M
- Stadler, Rudolf
- Leigh, Irene M
- Nürnberg, Peter
- Reis, André
- Hennies, Hans Christian
Producer: 20030226
In:
Human genetics vol. 112
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553.
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Molecular evidence of interhuman transmission of Pneumocystis pneumonia among renal transplant recipients hospitalized with HIV-infected patients. [electronic resource] by
- Rabodonirina, Meja
- Vanhems, Philippe
- Couray-Targe, Sandrine
- Gillibert, René-Pierre
- Ganne, Christell
- Nizard, Nathalie
- Colin, Cyrille
- Fabry, Jacques
- Touraine, Jean-Louis
- van Melle, Guy
- Nahimana, Aimable
- Francioli, Patrick
- Hauser, Philippe M
Producer: 20041213
In:
Emerging infectious diseases vol. 10
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554.
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Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis. [electronic resource] by
- Campeau, Philippe M
- Lu, James T
- Sule, Gautam
- Jiang, Ming-Ming
- Bae, Yangjin
- Madan, Simran
- Högler, Wolfgang
- Shaw, Nicholas J
- Mumm, Steven
- Gibbs, Richard A
- Whyte, Michael P
- Lee, Brendan H
Producer: 20130326
In:
Human molecular genetics vol. 21
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555.
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A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations. [electronic resource] by
- Pacheco-Cuéllar, Guillermo
- Gauthier, Julie
- Désilets, Valérie
- Lachance, Christian
- Lemire-Girard, Marlène
- Rypens, Françoise
- Le Deist, Françoise
- Decaluwe, Hélène
- Duval, Michel
- Bouron-Dal Soglio, Dorothée
- Kokta, Victor
- Haddad, Élie
- Campeau, Philippe M
Producer: 20180425
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 32
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556.
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Mutations in the phosphatidylinositol glycan C ( [electronic resource] by
- Edvardson, Simon
- Murakami, Yoshiko
- Nguyen, Thi Tuyet Mai
- Shahrour, Maher
- St-Denis, Anik
- Shaag, Avraham
- Damseh, Nadira
- Le Deist, Françoise
- Bryceson, Yenan
- Abu-Libdeh, Bassam
- Campeau, Philippe M
- Kinoshita, Taroh
- Elpeleg, Orly
Producer: 20171120
In:
Journal of medical genetics vol. 54
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557.
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[Problems posed for the anesthetist-resuscitator by aorto-coronary bypass surgery. Possible consequences of anesthesia. Attempts at prevention. Retrospective study of 353 cases]. [electronic resource] by
- Estanove, S
- Achkar, W
- Hamandjian, I
- Du Grès, B
- George, M
- Amouroux, C
- Deliry, P
- Pousset, M B
- Maret, H
- Samuel, D
- Philippe, M
- Boivin, J
- Brulé, P
- Cherfa, A
- Gressier, M
Producer: 19800514
In:
Annales de l'anesthesiologie francaise vol. 20
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558.
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FHF1 (FGF12) epileptic encephalopathy. [electronic resource] by
- Al-Mehmadi, Sameer
- Splitt, Miranda
- Ramesh, Venkateswaran
- DeBrosse, Suzanne
- Dessoffy, Kimberly
- Xia, Fan
- Yang, Yaping
- Rosenfeld, Jill A
- Cossette, Patrick
- Michaud, Jacques L
- Hamdan, Fadi F
- Campeau, Philippe M
- Minassian, Berge A
Publication details: Neurology. Genetics Dec 2016
In:
Neurology. Genetics vol. 2
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559.
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Silica gel solid nanocomposite electrolytes with interfacial conductivity promotion exceeding the bulk Li-ion conductivity of the ionic liquid electrolyte filler. [electronic resource] by
- Chen, Xubin
- Put, Brecht
- Sagara, Akihiko
- Gandrud, Knut
- Murata, Mitsuhiro
- Steele, Julian A
- Yabe, Hiroki
- Hantschel, Thomas
- Roeffaers, Maarten
- Tomiyama, Morio
- Arase, Hidekazu
- Kaneko, Yukihiro
- Shimada, Mikinari
- Mees, Maarten
- Vereecken, Philippe M
Publication details: Science advances 01 2020
In:
Science advances vol. 6
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560.
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Identification of novel mutations confirms PDE4D as a major gene causing acrodysostosis. [electronic resource] by
- Lynch, Danielle C
- Dyment, David A
- Huang, Lijia
- Nikkel, Sarah M
- Lacombe, Didier
- Campeau, Philippe M
- Lee, Brendan
- Bacino, Carlos A
- Michaud, Jacques L
- Bernier, Francois P
- Parboosingh, Jillian S
- Innes, A Micheil
Producer: 20130701
In:
Human mutation vol. 34
Availability: No items available.
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