Morphometric evaluation of the foramen magnum for sex determination: A study from Saudi Arabia von Madadin, Mohammed, Menezes, Ritesh G, Al Saif, Hind, Abo Alola, Hossain, Al Muhanna, Afnan, Gullenpet, Abid H, Nagesh, K.R, Kharoshah, Magdy A, Al Dhafery, Bander

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A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American von Dougherty, Sean C, Harper, Amy, Al Saif, Hind, Vorona, Gregory, Haines, Scott R

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Uterine and tubal abnormalities in infertile Saudi Arabian women: A teaching hospital experience von Al-Turki, Haifa, Gullenpet, Abid, Syed, Anjum, Al-Saif, Hind, Aldhafery, Bander

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A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations von Saif, Hind Al, Kanhere, Mansi, Wallace, Michael, Sahni, Dev R., Couser, Natario L.

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Unusual Presentation of Gianotti-Crosti Syndrome due to Epstein-Barr Virus Infection von Al Kaabi, Salwa, Al Kaabi, Aysha, Kara Hamo, Yasmin, Al Kaabi, Amani, Al Dhaheri, Hind Saif, Al Tatari, Hossam

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Multiloculated Cavitary Primary Pulmonary Hodgkin Lymphoma: Case Series von Aljehani, Yasser, Al-Saif, Hind, Al-Osail, Aisha, Al-Osail, Emad

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Case report of mosaic creatine transporter deficiency in a male pediatric patient von Brooks, Amy, Al Saif, Hind, McDermott, Emily

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Ocular Manifestations of the NAA10-Related Syndrome von Couser, Natario L., Lent, Jennifer M., Saif, Hind Al, Gupta, Angela S.

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Ophthalmic abnormalities in Wieacker-Wolff syndrome von Comlekoglu, Tien, Kumar, Virang, King, Kayla, Al Saif, Hind, Li, Rachel, Couser, Natario

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Eye, ocular adnexa, and facial manifestations of tetrasomy 18p: case report and literature review von Saadeh-Jackson, Stephanie, King, Kayla, Al Saif, Hind, Jackson-Cook, Colleen, Couser, Natario

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eP101 - Eye, ocular adnexa, and facial manifestations of tetrasomy 18p: case report and literature review von Saadeh-Jackson, Stephanie, King, Kayla, Al Saif, Hind, Jackson-Cook, Colleen, Couser, Natario

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Hereditary motor and sensory neuropathy type VIa with optic atrophy in two sisters with pathologic myopia: a case series and review von Seamon, Kimberly M., Jewell, Ann, Harrison, Anna, Harper, Amy, Al Saif, Hind, Couser, Natario L.

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Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay von Tan, Senwei, Zhang, Qiumeng, Zhan, Rui, Luo, Si, Han, Yaoling, Yu, Bin, Muss, Candace, Pingault, Veronique, Marlin, Sandrine, Delahaye, Andrée, Peters, Sophia, Perne, Claudia, Kreiß, Martina, Spataro, Nino, Trujillo-Quintero, Juan Pablo, Racine, Caroline, Tran-Mau-Them, Frederic, Phornphutkul, Chanika, Besterman, Aaron D, Martinez, Julian, Wang, Xiuxia, Tian, Xiaoyu, Srivastava, Siddharth, Urion, David K, Madden, Jill A, Saif, Hind Al, Morrow, Michelle M, Begtrup, Amber, Li, Xing, Jurgensmeyer, Sarah, Leahy, Peter, Zhou, Shimin, Li, Faxiang, Hu, Zhengmao, Tan, Jieqiong, Xia, Kun, Guo, Hui

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De novo variants in DENND5B cause a neurodevelopmental disorder von Scala, Marcello, Ferla, Matteo, Fatemi, Ali, Phillips, John A., Rio, Marlene, Siquier, Karine, Musante, Ilaria, Baldassari, Simona, Iacomino, Michele, Acosta, Maria T., Allworth, Aimee, Afzali, Ben, Bademci, Guney, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, HsiaoTuan, Chinn, Ivan, Clark, Gary D., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Fisher, Paul G., Fogel, Brent L., Gahl, William A., Glass, Ian, Godfrey, Rena A., Grajewski, Alana, Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, Hom, Jason, Huang, Alden, Introne, Wendy, Jarvik, Jeffrey, Jobanputra, Vaidehi, Kilich, Gonench, Kohler, Jennefer N., Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Marth, Gabor, Martin, Beth A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo, Morimoto, Marie, Nakano-Okuno, Mariko, Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Parker, Neil H., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Saporta, Mario, Schaechter, Judy, Seto, Elaine, Shelkowitz, Emily, Shin, Jimann, Solnica-Krezel, Lilianna, Sweetser, David A., Sybert, Virginia, Tarakad, Arjun, Velinder, Matt, Viskochil, Dave, Ward, Patricia A., Wegner, Daniel, Weisz Hubshman, Monika, Wener, Mark, Wenger, Tara, Reed, Sara, Al Saif, Hind, Walsh, Matthew B., Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Severino, Mariasavina

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Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis von Johnson, Janel O, Chia, Ruth, Miller, Danny E, Li, Rachel, Kumaran, Ravindran, Abramzon, Yevgeniya, Alahmady, Nada, Renton, Alan E, Topp, Simon D, Gibbs, J. Raphael, Cookson, Mark R, Sabir, Marya S, Dalgard, Clifton L, Troakes, Claire, Jones, Ashley R, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Ticozzi, Nicola, Silani, Vincenzo, Gellera, Cinzia, Blair, Ian P, Dobson-Stone, Carol, Kwok, John B, Bonkowski, Emily S, Palvadeau, Robin, Tienari, Pentti J, Morrison, Karen E, Shaw, Pamela J, Al-Chalabi, Ammar, Brown, Robert H, Calvo, Andrea, Mora, Gabriele, Al-Saif, Hind, Gotkine, Marc, Leigh, Fawn, Chang, Irene J, Perlman, Seth J, Glass, Ian, Scott, Anna, Shaw, Christopher E, Basak, A. Nazli, Landers, John E, Chio, Adriano, Crawford, Thomas O, Smith, Bradley N, Traynor, Bryan J

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Demographics and co‐occurring conditions in a clinic‐based cohort with Down syndrome in the United Arab Emirates von Corder, Jennifer Price, Al Ahbabi, Fatima Jaber Sehmi, Al Dhaheri, Hind Saif, Chedid, Fares

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Ocular Manifestations of the NAA10-Related Syndrome von Gupta, Angela S, Saif, Hind Al, Lent, Jennifer M, Couser, Natario L

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Multiloculated Cavitary Primary Pulmonary Hodgkin Lymphoma: Case Series von Aljehani, Yasser, Al-Saif, Hind, Al-Osail, Aisha, Al-Osail, Emad

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A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American von Dougherty, Sean C, Harper, Amy, Saif, Hind Al, Vorona, Gregory, Haines, Scott R

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A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American von Dougherty, Sean C, Harper, Amy, Al Saif, Hind, Vorona, Gregory, Haines, Scott R

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