Pesquisa | Biblioteca Virtual em Saúde

1.

Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.

Campbell, Ian M; Crowley, T Blaine; Jobaliya, Chintan; Bailey, Alice; McGinn, Daniel E; Gaiser, Kimberly; Bassett, Anne; Gur, Raquel E; Morrow, Bernice; Emanuel, Beverly S; Franco, Aime T; French, Deborah; Zackai, Elaine H; McDonald-McGinn, Donna M; Lambert, Michele P.

Clin Genet ; 103(1): 109-113, 2023 01.

Artigo em Inglês | MEDLINE | ID: mdl-36075864

2.

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.

Crowley, T Blaine; Campbell, Ian M; Liebling, Emily J; Lambert, Michele P; Levitt Katz, Lorraine E; Heimall, Jennifer; Bailey, Alice; McGinn, Daniel E; McDonald McGinn, Donna M; Sullivan, Kathleen E.

J Allergy Clin Immunol ; 149(1): 445-450, 2022 01.

Artigo em Inglês | MEDLINE | ID: mdl-34144109

3.

Cardiac evaluation of patients with 22q11.2 duplication syndrome.

Butensky, Adam; de Rinaldis, Chiara Pandolfi; Patel, Shrey; Edman, Sharon; Bailey, Alice; McGinn, Daniel E; Zackai, Elaine; Crowley, T Blaine; McDonald-McGinn, Donna M; Min, Jungwon; Goldmuntz, Elizabeth.

Am J Med Genet A ; 185(3): 753-758, 2021 03.

Artigo em Inglês | MEDLINE | ID: mdl-33369133

4.

Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome Without Intracardiac Anomalies.

de Rinaldis, Chiara Pandolfi; Butensky, Adam; Patel, Shrey; Edman, Sharon; Wasserman, Melissa; McGinn, Daniel E; Bailey, Alice; Zackai, Elaine H; Crowley, T Blaine; McDonald-McGinn, Donna M; Min, Jungwon; Goldmuntz, Elizabeth.

Pediatr Cardiol ; 42(7): 1594-1600, 2021 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-34128123

5.

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.

Campbell, Ian M; Sheppard, Sarah E; Crowley, T Blaine; McGinn, Daniel E; Bailey, Alice; McGinn, Michael J; Unolt, Marta; Homans, Jelle F; Chen, Erin Y; Salmons, Harold I; Gaynor, J William; Goldmuntz, Elizabeth; Jackson, Oksana A; Katz, Lorraine E; Mascarenhas, Maria R; Deeney, Vincent F X; Castelein, René M; Zur, Karen B; Elden, Lisa; Kallish, Staci; Kolon, Thomas F; Hopkins, Sarah E; Chadehumbe, Madeline A; Lambert, Michele P; Forbes, Brian J; Moldenhauer, Julie S; Schindewolf, Erica M; Solot, Cynthia B; Moss, Edward M; Gur, Raquel E; Sullivan, Kathleen E; Emanuel, Beverly S; Zackai, Elaine H; McDonald-McGinn, Donna M.

Am J Med Genet A ; 176(10): 2058-2069, 2018 10.

Artigo em Inglês | MEDLINE | ID: mdl-30380191

6.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.

Delio, Maria; Guo, Tingwei; McDonald-McGinn, Donna M; Zackai, Elaine; Herman, Sean; Kaminetzky, Mark; Higgins, Anne Marie; Coleman, Karlene; Chow, Carolyn; Jalbrzikowski, Maria; Jarlbrzkowski, Maria; Bearden, Carrie E; Bailey, Alice; Vangkilde, Anders; Olsen, Line; Olesen, Charlotte; Skovby, Flemming; Werge, Thomas M; Templin, Ludivine; Busa, Tiffany; Philip, Nicole; Swillen, Ann; Vermeesch, Joris R; Devriendt, Koen; Schneider, Maude; Dahoun, Sophie; Eliez, Stephan; Schoch, Kelly; Hooper, Stephen R; Shashi, Vandana; Samanich, Joy; Marion, Robert; van Amelsvoort, Therese; Boot, Erik; Klaassen, Petra; Duijff, Sasja N; Vorstman, Jacob; Yuen, Tracy; Silversides, Candice; Chow, Eva; Bassett, Anne; Frisch, Amos; Weizman, Abraham; Gothelf, Doron; Niarchou, Maria; van den Bree, Marianne; Owen, Michael J; Suñer, Damian Heine; Andreo, Jordi Rosell; Armando, Marco.

Am J Hum Genet ; 92(3): 439-47, 2013 Mar 07.

Artigo em Inglês | MEDLINE | ID: mdl-23453669

7.

Increased T-cell counts in patients with 22q11.2 deletion syndrome who have anxiety.

Dou, Ying; Blaine Crowley, T; Gallagher, Sean; Bailey, Alice; McGinn, Daniel; Zackai, Elaine; Gur, Raquel E; McGinn, Donna McDonald; Sullivan, Kathleen E.

Am J Med Genet A ; 182(7): 1815-1818, 2020 07.

Artigo em Inglês | MEDLINE | ID: mdl-32302047

8.

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.

McDonald-McGinn, Donna M; Fahiminiya, Somayyeh; Revil, Timothée; Nowakowska, Beata A; Suhl, Joshua; Bailey, Alice; Mlynarski, Elisabeth; Lynch, David R; Yan, Albert C; Bilaniuk, Larissa T; Sullivan, Kathleen E; Warren, Stephen T; Emanuel, Beverly S; Vermeesch, Joris R; Zackai, Elaine H; Jerome-Majewska, Loydie A.

J Med Genet ; 50(2): 80-90, 2013 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-23231787

9.

Case report: Advice for schools on managing functional tic-like behaviours.

Owen, Tamsin; Silva, Juliana; Grose, Claire; Bailey, Alice; Robinson, Sally; Anderson, Seonaid; Ludlow, Amanda; Sharp, Sarah; Toghill, Lucy; Hedderly, Tammy.

Front Psychiatry ; 13: 1001459, 2022.

Artigo em Inglês | MEDLINE | ID: mdl-36545035

10.

A novel decision aid to help plan for serious illness: a multisite randomized trial.

Heyland, Daren K; Heyland, Rebecca; Bailey, Alice; Howard, Michelle.

CMAJ Open ; 8(2): E289-E296, 2020.

Artigo em Inglês | MEDLINE | ID: mdl-32345707

11.

Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic procedures.

Kimia, Rotem; Elden, Lisa; Dailey, Julia; Kodavatiganti, Mallika; Crowley, T Blaine; McGinn, Daniel E; Bailey, Alice; Zackai, Elaine H; McDonald-McGinn, Donna M; Jackson, Oksana A.

Int J Pediatr Otorhinolaryngol ; 138: 110236, 2020 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-32890936

12.

Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR).

Pastor, Steven; Tran, Oanh; Jin, Andrea; Carrado, Danielle; Silva, Benjamin A; Uppuluri, Lahari; Abid, Heba Z; Young, Eleanor; Crowley, T Blaine; Bailey, Alice G; McGinn, Daniel E; McDonald-McGinn, Donna M; Zackai, Elaine H; Xie, Michael; Taylor, Deanne; Morrow, Bernice E; Xiao, Ming; Emanuel, Beverly S.

Sci Rep ; 10(1): 12235, 2020 07 22.

Artigo em Inglês | MEDLINE | ID: mdl-32699385

13.

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.

Wenger, Tara L; Kao, Charlly; McDonald-McGinn, Donna M; Zackai, Elaine H; Bailey, Alice; Schultz, Robert T; Morrow, Bernice E; Emanuel, Beverly S; Hakonarson, Hakon.

Sci Rep ; 6: 19372, 2016 Jan 19.

Artigo em Inglês | MEDLINE | ID: mdl-26781481

14.

Data use under the NIH GWAS data sharing policy and future directions.

Paltoo, Dina N; Rodriguez, Laura Lyman; Feolo, Michael; Gillanders, Elizabeth; Ramos, Erin M; Rutter, Joni L; Sherry, Stephen; Wang, Vivian Ota; Bailey, Alice; Baker, Rebecca; Caulder, Mark; Harris, Emily L; Langlais, Kristofor; Leeds, Hilary; Luetkemeier, Erin; Paine, Taunton; Roomian, Tamar; Tryka, Kimberly; Patterson, Amy; Green, Eric D.

Nat Genet ; 46(9): 934-8, 2014 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-25162809

15.

Tratado sobre slos siete rayos: psicología esotérica

Bailey, Alice Anne.

Buenos Aires; Fundación Lucis; 1a. ed; 1959. 561 p. 23 cm. (76900).

Monografia em Espanhol | BINACIS | ID: bin-76900

16.

Tratado sobre slos siete rayos: psicología esotérica

Bailey, Alice Anne.

Buenos Aires; Fundación Lucis; 1a. ed; 1959. 561 p. ^e23 cm.

Monografia em Espanhol | LILACS-Express | ID: biblio-1200718

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Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.

Cardiac evaluation of patients with 22q11.2 duplication syndrome.

Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome Without Intracardiac Anomalies.

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.

Increased T-cell counts in patients with 22q11.2 deletion syndrome who have anxiety.

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.

Case report: Advice for schools on managing functional tic-like behaviours.

A novel decision aid to help plan for serious illness: a multisite randomized trial.

Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic procedures.

Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR).

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.

Data use under the NIH GWAS data sharing policy and future directions.

Tratado sobre slos siete rayos: psicología esotérica

Tratado sobre slos siete rayos: psicología esotérica