Utilization and metabolism of urea during spore germination by Geotrichum candidum von Shorer, J., Zelmanowicz, Ilana, Barash, I.

Volltext

High-Molecular-Weight Serum Thyrotropin Revisited von Bifulco, M, Spitz, I, Hirsch, H J, Shorer, J, Aloj, S M

Volltext

All-optical reporting of inhibitory receptor driving force in the nervous system von Selfe, Joshua S., Steyn, Teresa J. S., Shorer, Eran F., Burman, Richard J., Düsterwald, Kira M., Kraitzick, Ariel Z., Abdelfattah, Ahmed S., Schreiter, Eric R., Newey, Sarah E., Akerman, Colin J., Raimondo, Joseph V.

Volltext

The Montreal Cognitive Assessment Test (MoCA) as a screening tool for cognitive dysfunction in fibromyalgia von Elkana, Odelia, Nimni, Yael, Ablin, Jacob N, Shorer, Ran, Aloush, Valerie

Volltext

Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 von Barel, Ortal, Shalev, Stavit A., Ofir, Rivka, Cohen, Asi, Zlotogora, Joel, Shorer, Zamir, Mazor, Galia, Finer, Gal, Khateeb, Shareef, Zilberberg, Noam, Birk, Ohad S.

Volltext

Retinal nerve fiber layer thickness and neuropsychiatric manifestations in systemic lupus erythematosus von Shulman, S, Shorer, R, Wollman, J, Dotan, G, Paran, D

Volltext

A modified version of the 2016 ACR fibromyalgia criteria cognitive items results in stronger correlations between subjective and objective measures of cognitive impairment von Elkana, Odelia, Yaalon, Chen, Raev, Sheer, Sobol, Noy, Ablin, Jacob N, Shorer, Ran, Aloush, Valerie

Volltext

Tryptophan-kynurenine metabolic pathway and daytime dysfunction in women with HIV von Shorer, Eran Frank, Rubin, Leah H, French, Audrey L, Weber, Kathleen M, Daubert, Elizabeth, Yohannes, Tsion, Morack, Ralph, Clish, Clary, Bullock, Kevin, Gustafson, Deborah, Sharma, Anjali, Rogando, Andrea C, Qi, Qibin, Burgess, Helen J, Dastgheyb, Raha M

Volltext

Does the cognitive index of the symptom severity scale evaluate cognition? Data from subjective and objective cognitive measures in fibromyalgia von Elkana, Odelia, Falcofsky, Amir K, Shorer, Ran, Bar-On Kalfon, Tamar, Ablin, Jacob N

Volltext

P835: GENETIC BACKGROUND AND CLINICAL CHARACTERISTICS OF CONGENITAL NEUTROPENIAS IN ISRAEL von Steinberg‐Shemer, O., Yeshareem, L., Noy‐Lotan, S., Dgany, O., Krasnov, T., Berger Pinto, G., Bielorai, B., Kuperman, A. A., Laor, R., Mandel‐Shorer, N., Ben Barak, A., Levin, C., Mahdi, A., Miskin, H., Revel‐Vilk, S., Levin, D., Benish, M., Zuckerman, T., Wolach, O., Pazgal, I., Gilad, O., Goldberg, T., Yacobovich, J., Izraeli, S., Tamary, H.

Volltext

P817: SYNDROMES PREDISPOSING TO LEUKEMIA ARE A MAJOR CAUSE OF INHERITED CYTOPENIAS IN CHILDREN von Gilad, O., Dgany, O., Noy ‐Lotan, S., Krasnov, T., Yacobovich, J., Rabinowicz, R., Goldberg, T., Kuperman, A., Abu‐Quider, A., Miskin, H., Kapelushnik, N., Mandel‐Shorer, N., Shimony, S., Harlev, D., Ben‐Ami, T., Adam, E., Levin, C., Aviner, S., Elhasid, R., Berger‐Achituv, S., Chaitman‐Yerushalmi, L., Kodman, Y., Oniashvilli, N., Hameiri‐ Grosman, M., Izraeli, S., Tamary, H., Steinberg‐Shemer, O.

Volltext

Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations von Cox, James J, Sheynin, Jony, Shorer, Zamir, Reimann, Frank, Nicholas, Adeline K, Zubovic, Lorena, Baralle, Marco, Wraige, Elizabeth, Manor, Esther, Levy, Jacov, Woods, C. Geoffery, Parvari, Ruti

Volltext

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization von Afawi, Zaid, Oliver, Karen L, Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y, Helbig, Katherine L, Goldberg-Stern, Hadassa, Misk, Adel J, Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H, Mangelsdorf, Marie, MacPherson, James N, Carvill, Gemma L, Mefford, Heather C, Jackson, Graeme D, Scheffer, Ingrid E, Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E, Corbett, Mark, Mulley, John C, Dibbens, Leanne M, Korczyn, Amos D, Berkovic, Samuel F

Volltext

Estradiol supplementation during the luteal phase may improve the pregnancy rate in patients undergoing in vitro fertilization-embryo transfer cycles von Farhi, Jacob, Weissman, Ariel, Steinfeld, Zohar, Shorer, Michal, Nahum, Hana, Levran, David

Volltext

Nerve growth factor-tyrosine kinase A pathway is involved in thermoregulation and adaptation to stress: studies on patients with hereditary sensory and autonomic neuropathy type IV von Loewenthal, Neta, Levy, Jacov, Schreiber, Ruth, Pinsk, Vered, Perry, Zvi, Shorer, Zamir, Hershkovitz, Eli

Volltext

Familial infantile bilateral striatal necrosis: Clinical features and response to biotin treatment von STRAUSSBERG, R, SHORER, Z, WEITZ, R, BASEL, L, KORNREICH, L, COIRE, C. I, HAREL, L, DJALDETTI, R, AMIR, J

Volltext

Demyelinating Peripheral Neuropathy in Merosin-Deficient Congenital Muscular Dystrophy von Shorer, Zamir, Philpot, Joanne, Muntoni, Francesco, Sewry, Caroline, Dubowitz, Victor

Volltext

Congenital insensitivity to pain with anhidrosis: ocular and systemic manifestations von Yagev, Ronit, Levy, Jacov, Shorer, Zamir, Lifshitz, Tova

Volltext

Point-of-Use Mixing of Influenza H5N1 Vaccine and MF59 Adjuvant for Pandemic Vaccination Preparedness: Antibody Responses and Safety. A Phase 1 Clinical Trial von Mulligan, Mark J., Bernstein, David I., Frey, Sharon, Winokur, Patricia, Rouphael, Nadine, Dickey, Michelle, Edupuganti, Srilatha, Spearman, Paul, Anderson, Edwin, Graham, Irene, Noah, Diana L., Mangal, Brian, Kim, Sonnie, Hill, Heather

Volltext

Neurophysiologic studies in congenital insensitivity to pain with anhidrosis von Shorer, Zamir, Moses, Shimon W, Hershkovitz, Eliahu, Pinsk, Vered, Levy, Jacov

Volltext