Stable non-Robertsonian dicentric chromosomes: four new cases and a review von LEMYRE, EMMANUELLE, KALOUSTIAN, VAZKEN M DER, DUNCAN, ALESSANDRA M V

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Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems von Williams, Stephen R., Aldred, Micheala A., Der Kaloustian, Vazken M., Halal, Fahed, Gowans, Gordon, McLeod, D. Ross, Zondag, Sara, Toriello, Helga V., Magenis, R. Ellen, Elsea, Sarah H.

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Mortality and losses to follow‐up among adolescents living with HIV in the IeDEA global cohort collaboration von Kariminia, Azar, Law, Matthew, Davies, Mary‐Ann, Vinikoor, Michael, Wools‐Kaloustian, Kara, Leroy, Valeriane, Edmonds, Andrew, McGowan, Catherine, Vreeman, Rachel, Fairlie, Lee, Ayaya, Samuel, Yotebieng, Marcel, Takassi, Elom, Pinto, Jorge, Adedimeji, Adebola, Malateste, Karen, Machado, Daisy M, Penazzato, Martina, Hazra, Rohan, Sohn, Annette H

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Deletion of 22qll in two brothers with different phenotype von KASPRZAK, L, KALOUSTIAN, V. M. D, ELLIOTT, A. M, SHEVELL, M, LEJTENYI, C, EYDOUX, P

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Juvenile hyaline fibromatosis: Two new patients and review of the literature von Fayad, Michel N., Yacoub, Antoine, Salman, Salah, Khudr, Adele, Der Kaloustian, Vazken M., Opitz, John M., Reynolds, James F.

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Positional cloning of the gene for Nijmegen breakage syndrome von Matsuura, Shinya, Tauchi, Hiroshi, Nakamura, Asako, Kondo, Noriko, Sakamoto, Shuichi, Endo, Satoru, Smeets, Dominique, Solder, Brigitte, Belohradsky, Bernd H., Der Kaloustian, Vazken M., Oshimura, Mitsuo, Isomura, Minoru, Nakamura, Yusuke, Komatsu, Kenshi

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Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23 von Bork, Julie M., Peters, Linda M., Riazuddin, Saima, Bernstein, Steve L., Ahmed, Zubair M., Ness, Seth L., Polomeno, Robert, Ramesh, Arabandi, Schloss, Melvin, Srisailpathy, C. R. Srikumari, Wayne, Sigrid, Bellman, Susan, Desmukh, Dilip, Ahmed, Zahoor, Khan, Shaheen N., Kaloustian, Vazken M. Der, Li, X. Cindy, Lalwani, Anil, Riazuddin, Sheikh, Bitner-Glindzicz, Maria, Nance, Walter E., Liu, Xue-Zhong, Wistow, Graeme, Smith, Richard J.H., Griffith, Andrew J., Wilcox, Edward R., Friedman, Thomas B., Morell, Robert J.

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The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis von Slogrove, Amy L, Schomaker, Michael, Davies, Mary-Ann, Williams, Paige, Balkan, Suna, Ben-Farhat, Jihane, Calles, Nancy, Chokephaibulkit, Kulkanya, Duff, Charlotte, Eboua, Tanoh François, Kekitiinwa-Rukyalekere, Adeodata, Maxwell, Nicola, Pinto, Jorge, Seage, 3rd, George, Teasdale, Chloe A, Wanless, Sebastian, Warszawski, Josiane, Wools-Kaloustian, Kara, Yotebieng, Marcel, Timmerman, Venessa, Collins, Intira J, Goodall, Ruth, Smith, Colette, Patel, Kunjal, Paul, Mary, Gibb, Diana, Vreeman, Rachel, Abrams, Elaine J, Hazra, Rohan, Van Dyke, Russell, Bekker, Linda-Gail, Mofenson, Lynne, Vicari, Marissa, Essajee, Shaffiq, Penazzato, Martina, Anabwani, Gabriel, Q Mohapi, Edith, N Kazembe, Peter, Hlatshwayo, Makhosazana, Lumumba, Mwita, Goetghebuer, Tessa, Thorne, Claire, Galli, Luisa, van Rossum, Annemarie, Giaquinto, Carlo, Marczynska, Magdalena, Marques, Laura, Prata, Filipa, Ene, Luminita, Okhonskaia, Liubov, Rojo, Pablo, Fortuny, Claudia, Naver, Lars, Rudin, Christoph, Le Coeur, Sophie, Volokha, Alla, Rouzier, Vanessa, Succi, Regina, Sohn, Annette, Kariminia, Azar, Edmonds, Andrew, Lelo, Patricia, Ayaya, Samuel, Ongwen, Patricia, Jefferys, Laura F, Phiri, Sam, Mubiana-Mbewe, Mwangelwa, Sawry, Shobna, Renner, Lorna, Sylla, Mariam, Abzug, Mark J, Levin, Myron, Oleske, James, Chernoff, Miriam, Traite, Shirley, Purswani, Murli, Chadwick, Ellen G, Judd, Ali, Leroy, Valériane

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Estimation of mortality among HIV-infected people on antiretroviral treatment in east Africa: a sampling based approach in an observational, multisite, cohort study von Geng, Elvin H, Dr, Odeny, Thomas A, MBChB, Lyamuya, Rita E, MBChB, Nakiwogga-Muwanga, Alice, MMed, Diero, Lameck, Prof, Bwana, Mwebesa, MBChB, Muyindike, Winnie, MMed, Braitstein, Paula, PhD, Somi, Geoffrey R, MD, Kambugu, Andrew, MMed, Bukusi, Elizabeth A, Prof, Wenger, Megan, MPH, Wools-Kaloustian, Kara K, Prof, Glidden, David V, Prof, Yiannoutsos, Constantin T, Prof, Martin, Jeffrey N, Prof

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Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome von Diaz-Meyer, N, Day, C D, Khatod, K, Maher, E R, Cooper, W, Reik, W, Junien, C, Graham, G, Algar, E, Der Kaloustian, V M, Higgins, M J

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The role of dermatology in Kaposi sarcoma diagnosis across three regions in sub-Saharan Africa: J Am Acad Dermatol von Seth, D., Williams, V. L., Mcmahon, D. E., Regan, S., Busakhala, N., Wools-Kaloustian, K., Mosoajane, K., Ralefala, T. B., Kayembe, M., Iregbu, K., Kwaghe, V., Jedy-Agba, E., Oyesiku, L., Maurer, T., Jaquet, Antoine, Bassett, I. V., Martin, J., Grover, S., Freeman, E. E.

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The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes von Laloi-Michelin, M., Meas, T., Ambonville, C., Bellanné-Chantelot, C., Beaufils, S., Massin, P., Vialettes, B., Gin, H., Timsit, J., Bauduceau, B., Bernard, L., Bertin, E., Blickle, J.-F., Cahen-Varsaux, J., Cailleba, A., Casanova, S., Cathebras, P., Charpentier, G., Chedin, P., Crea, T., Delemer, B, Dubois-Laforgue, D., Duchemin, F., Ducluzeau, P. H., Bouhanick, B., Dusselier, L., Gabreau, T., Grimaldi, A., Guerci, B., Jacquin, V., Kaloustian, E., Larger, E., Lecleire-Collet, A., Lorenzini, F., Louis, J., Mausset, J., Murat, A., Nadler-Fluteau, S., Olivier, F., Paquis-Flucklinger, V., Paris-Bockel, D., Raynaud, I., Reznik, Y., Riveline, J. P., Schneebeli, S., Sonnet, E., Sola-Gazagnes, A., Thomas, J. L., Trabulsi, B., Virally, M., Guillausseau, P. J.

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A call to incorporate the prevention and treatment of geriatric disorders in the management of diabetes in the elderly von Vischer, U.-M, Bauduceau, B, Bourdel-Marchasson, I, Blickle, J.-F, Constans, T, Fagot-Campagna, A, Kaloustian, E, Lassman-Vague, V, Lecomte, P, Simon, D, Tessier, D, Verny, C, Doucet, J

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Clinical Characteristics and Diagnostic Criteria of Maturity-Onset Diabetes Of The Young (MODY) due to Molecular Anomalies of the HNF1A Gene von Bellanné-Chantelot, Christine, Lévy, David Joseph, Carette, Claire, Saint-Martin, Cécile, Riveline, Jean-Pierre, Larger, Etienne, Valéro, René, Gautier, Jean-François, Reznik, Yves, Sola, Agnès, Hartemann, Agnès, Laboureau-Soares, Sandrine, Laloi-Michelin, Marie, Lecomte, Pierre, Chaillous, Lucy, Dubois-Laforgue, Danièle, Timsit, José, on behalf of the French Monogenic Diabetes Study Group

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A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family von Rivière, Jean-Baptiste, Verlaan, Dominique J., Shekarabi, Masoud, Lafrenière, Ronald G., Bénard, Mélanie, Der Kaloustian, Vazken M., Shbaklo, Zuhayr, Rouleau, Guy A.

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Nijmegen breakage syndrome von The, I

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Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B ( HNF1B ) molecular defects von Dubois-Laforgue, D, Bellanné-Chantelot, C, Charles, P, Jacquette, A, Larger, E, Ciangura, C, Saint-Martin, C, Rastel, C, Keren, B, Timsit, J

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Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study von Massin, P, Dubois-Laforgue, D, Meas, T, Laloi-Michelin, M, Gin, H, Bauduceau, B, Bellanné-Chantelot, C, Bertin, E, Blickle, J.-F, Bouhanick, B, Cahen-Varsaux, J, Casanova, S, Charpentier, G, Chedin, P, Dupuy, O, Grimaldi, A, Guerci, B, Kaloustian, E, Lecleire-Collet, A, Lorenzini, F, Murat, A, Narbonne, H, Olivier, F, Paquis-Flucklinger, V, Virally, M, Vincenot, M, Vialettes, B, Timsit, J, Guillausseau, P. J

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Mutations in GJB6 cause hidrotic ectodermal dysplasia von Lamartine, J, Munhoz Essenfelder, G, Kibar, Z, Lanneluc, I, Callouet, E, Laoudj, D, Lemaître, G, Hand, C, Hayflick, S J, Zonana, J, Antonarakis, S, Radhakrishna, U, Kelsell, D P, Christianson, A L, Pitaval, A, Der Kaloustian, V, Fraser, C, Blanchet-Bardon, C, Rouleau, G A, Waksman, G

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Predicting factors of hypoglycaemia in elderly type 2 diabetes patients: Contributions of the GERODIAB study von Bordier, L, Buysschaert, M, Bauduceau, B, Doucet, J, Verny, C, Lassmann Vague, V, Le Floch, J.P

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