Zoekresultaten - Morgan, Thomas M.

The education and medical practice of Dr. James McCune Smith (1813-1865), first black American to hold a medical degree. door Morgan, Thomas M.

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Mouse models of patent ductus arteriosus (PDA) and their relevance for human PDA door Yarboro, Michael T., Gopal, Srirupa H., Su, Rachel L., Morgan, Thomas M., Reese, Jeff

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Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome door Morgan, Thomas M, Xiao, Lan, Lyons, Patrick, Kassebaum, Bethany, Krumholz, Harlan M, Spertus, John A

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Genetic Risk Score Does Not Correlate with Body Mass Index of Latina Women in a Clinical Trial door Coenen, Kimberly R., Karp, Sharon M., Gesell, Sabina B., Dietrich, Mary S., Morgan, Thomas M., Barkin, Shari L.

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Vaccines Are Not Associated With Metabolic Events in Children With Urea Cycle Disorders door Morgan, Thomas M., Schlegel, Cameron, Edwards, Kathryn M., Welch-Burke, Teresa, Zhu, Yuwei, Sparks, Robert, Summar, Marshall

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Consanguinity Mapping of Congenital Heart Disease in a South Indian Population door McGregor, Tracy L., Misri, Amit, Bartlett, Jackie, Orabona, Guilherme, Friedman, Richard D., Sexton, David, Maheshwari, Sunita, Morgan, Thomas M.

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Liver Transplantation in Children with Urea Cycle Disorders: The Importance of Minimizing Waiting Time door Ziogas, Ioannis A., Wu, W. Kelly, Matsuoka, Lea K., Pai, Anita K., Hafberg, Einar T., Gillis, Lynette A., Morgan, Thomas M., Alexopoulos, Sophoclis P.

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Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype door McGregor, Tracy L, Gurnett, Christina A, Dobbs, Matthew B, Wise, Carol A, Morcuende, Jose A, Morgan, Thomas M, Menon, Ramkumar, Muglia, Louis J

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Adverse Fetal Outcomes Associated with Immunosuppressive Medications for Chronic Immune Mediated Diseases in Pregnancy door Cooper, William O., Cheetham, T. Craig, Li, De-Kun, Stein, C. Michael, Callahan, S. Todd, Morgan, Thomas M., Shintani, Ayumi K., Chen, Ning, Griffin, Marie R., Ray, Wayne A.

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A balanced t(10;15) translocation in a male patient with developmental language disorder door Ercan-Sencicek, A. Gulhan, Davis Wright, Nicole R., Sanders, Stephan J., Oakman, Nicole, Valdes, Lianna, Bakkaloglu, Betul, Doyle, Niamh, Yrigollen, Carolyn M., Morgan, Thomas M., Grigorenko, Elena L.

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Variation in Recovery: Role of Gender on Outcomes of Young AMI Patients (VIRGO) Study Design door Lichtman, Judith H., Lorenze, Nancy P., D’Onofrio, Gail, Spertus, John A., Lindau, Stacy T., Morgan, Thomas M., Herrin, Jeph, Bueno, Héctor, Mattera, Jennifer A., Ridker, Paul M., Krumholz, Harlan M.

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Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype door State, Matthew W., Greally, John M., Cuker, Adam, Bowers, Peter N., Henegariu, Octavian, Morgan, Thomas M., Gunel, Murat, DiLuna, Michael, King, Robert A., Nelson, Carol, Donovan, Abigail, Anderson, George M., Leckman, James F., Hawkins, Trevor, Pauls, David L., Lifton, Richard P., Ward, David C.

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Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome door Morgan, Thomas M, House, John A, Cresci, Sharon, Jones, Philip, Allayee, Hooman, Hazen, Stanley L, Patel, Yesha, Patel, Riyaz S, Eapen, Danny J, Waddy, Salina P, Quyyumi, Arshed A, Kleber, Marcus E, März, Winfried, Winkelmann, Bernhard R, Boehm, Bernhard O, Krumholz, Harlan M, Spertus, John A

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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans door Ercan-Sencicek, A Gulhan, Jambi, Samira, Franjic, Daniel, Nishimura, Sayoko, Li, Mingfeng, El-Fishawy, Paul, Morgan, Thomas M, Sanders, Stephan J, Bilguvar, Kaya, Suri, Mohnish, Johnson, Michele H, Gupta, Abha R, Yuksel, Zafer, Mane, Shrikant, Grigorenko, Elena, Picciotto, Marina, Alberts, Arthur S, Gunel, Murat, Šestan, Nenad, State, Matthew W

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Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders door Bakkaloglu, Betul, O'Roak, Brian J., Louvi, Angeliki, Gupta, Abha R., Abelson, Jesse F., Morgan, Thomas M., Chawarska, Katarzyna, Klin, Ami, Ercan-Sencicek, A. Gulhan, Stillman, Althea A., Tanriover, Gamze, Abrahams, Brett S., Duvall, Jackie A., Robbins, Elissa M., Geschwind, Daniel H., Biederer, Thomas, Gunel, Murat, Lifton, Richard P., State, Matthew W.

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USP7 acts as a molecular rheostat to promote WASH-dependent endosomal protein recycling and is mutated in a human neurodevelopmental disorder door Hao, Yi-Heng, Fountain, Michael D., Tacer, Klementina Fon, Xia, Fan, Bi, Weimin, Kang, Sung-Hae L., Patel, Ankita, Rosenfeld, Jill A., Caignec, Cédric Le, Isidor, Bertrand, Krantz, Ian D., Noon, Sarah E., Pfotenhauer, Jean P., Morgan, Thomas M., Moran, Rocio, Pedersen, Robert C., Saenz, Margarita S., Schaaf, Christian P., Potts, Patrick Ryan

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l-Histidine Decarboxylase and Tourette's Syndrome door Ercan-Sencicek, A. Gulhan, Stillman, Althea A., Ghosh, Ananda K., Bilguvar, Kaya, O'Roak, Brian J., Mason, Christopher E., Abbott, Thomas, Gupta, Abha, King, Robert A., Pauls, David L., Tischfield, Jay A., Heiman, Gary A., Singer, Harvey S., Gilbert, Donald L., Hoekstra, Pieter J., Morgan, Thomas M., Loring, Erin, Yasuno, Katsuhito, Fernandez, Thomas, Sanders, Stephan, Louvi, Angeliki, Cho, Judy H., Mane, Shrikant, Colangelo, Christopher M., Biederer, Thomas, Lifton, Richard P., Gunel, Murat, State, Matthew W.

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Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families door Ngcungcu, Thandiswa, Oti, Martin, Sitek, Jan C., Haukanes, Bjørn I., Linghu, Bolan, Bruccoleri, Robert, Stokowy, Tomasz, Oakeley, Edward J., Yang, Fan, Zhu, Jiang, Sultan, Marc, Schalkwijk, Joost, van Vlijmen-Willems, Ivonne M.J.J., von der Lippe, Charlotte, Brunner, Han G., Ersland, Kari M., Grayson, Wayne, Buechmann-Moller, Stine, Sundnes, Olav, Nirmala, Nanguneri, Morgan, Thomas M., van Bokhoven, Hans, Steen, Vidar M., Hull, Peter R., Szustakowski, Joseph, Staedtler, Frank, Zhou, Huiqing, Fiskerstrand, Torunn, Ramsay, Michele

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Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes door Hufnagel, Robert B, Arno, Gavin, Hein, Nichole D, Hersheson, Joshua, Prasad, Megana, Anderson, Yvonne, Krueger, Laura A, Gregory, Louise C, Stoetzel, Corinne, Jaworek, Thomas J, Hull, Sarah, Li, Abi, Plagnol, Vincent, Willen, Christi M, Morgan, Thomas M, Prows, Cynthia A, Hegde, Rashmi S, Riazuddin, Saima, Grabowski, Gregory A, Richardson, Rudy J, Dieterich, Klaus, Huang, Taosheng, Revesz, Tamas, Martinez-Barbera, J P, Sisk, Robert A, Jefferies, Craig, Houlden, Henry, Dattani, Mehul T, Fink, John K, Dollfus, Helene, Moore, Anthony T, Ahmed, Zubair M

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Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies door Fountain, Michael D., Oleson, David S., Rech, Megan E., Segebrecht, Lara, Hunter, Jill V., McCarthy, John M., Lupo, Philip J., Holtgrewe, Manuel, Moran, Rocio, Rosenfeld, Jill A., Isidor, Bertrand, Le Caignec, Cédric, Saenz, Margarita S., Pedersen, Robert C., Morgan, Thomas M., Pfotenhauer, Jean P., Xia, Fan, Bi, Weimin, Kang, Sung-Hae L., Patel, Ankita, Krantz, Ian D., Raible, Sarah E., Smith, Wendy, Cristian, Ingrid, Torti, Erin, Juusola, Jane, Millan, Francisca, Wentzensen, Ingrid M., Person, Richard E., Küry, Sébastien, Bézieau, Stéphane, Uguen, Kévin, Férec, Claude, Munnich, Arnold, van Haelst, Mieke, Lichtenbelt, Klaske D., van Gassen, Koen, Hagelstrom, Tanner, Chawla, Aditi, Perry, Denise L., Taft, Ryan J., Jones, Marilyn, Masser-Frye, Diane, Dyment, David, Venkateswaran, Sunita, Li, Chumei, Escobar, Luis F., Horn, Denise, Spillmann, Rebecca C., Peña, Loren, Wierzba, Jolanta, Strom, Tim M., Parenti, Ilaria, Kaiser, Frank J., Ehmke, Nadja, Schaaf, Christian P.

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