Soliman Alkrinawi

h-index

Research activity per year

Fingerprint

Dive into the research topics where Soliman Alkrinawi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

1 Similar Profiles

18 Article
1 Letter

Pediatric thermal epiglottitis: insights from a tertiary center experience
Slanovic, L., Arwas, N., Aviram, M., Gatt, D., Lazar, I., Feinstein, Y., Yafit, D., Goldbart, A., Alkrinawi, S., Golan-Tripto, I. & Neeman, E., 1 Jul 2024, In: European Journal of Pediatrics. 183, 7, p. 2913-2919 7 p.
Research output: Contribution to journal › Article › peer-review
1 Citation (Web of Science)
Stepwise genetic approach for the diagnosis of primary ciliary dyskinesia in highly consanguineous populations
Gatt, D., Tripto, I. G., Levanon, E., Arwas, N., Hazan, G., Alkrinawi, S., Goldbart, A. D. & Aviram, M., 1 May 2024, In: Archives of Disease in Childhood. 109, 5, p. 428-431 4 p.
Research output: Contribution to journal › Article › peer-review
6 Citations (Web of Science)
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening
Behar, D. M., Inbar, O., Shteinberg, M., Gur, M., Mussaffi, H., Shoseyov, D., Ashkenazi, M., Alkrinawi, S., Bormans, C., Hakim, F., Mei-Zahav, M., Cohen-Cymberknoh, M., Dagan, A., Prais, D., Sarouk, I., Stafler, P., Bar Aluma, B. E., Akler, G., Picard, E. & Aviram, M. & 7 others, Efrati, O., Livnat, G., Rivlin, J., Bentur, L., Blau, H., Kerem, E. & Singer, A., 1 May 2017, In: Molecular Genetics and Genomic Medicine. 5, 3, p. 223-236 14 p.
Research output: Contribution to journal › Article › peer-review

Open Access
10 Scopus citations
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities.
Amirav, I., Roberts, M. R., Mussaffi, H., Mandelberg, A., Roth, Y., Abitbul, R., Luder, A., Blau, H., Alkrinawi, S., Aviram, M., Ben-Ami, M., Rotschild, M., Bentur, L., Shoseyov, D., Cohen-Cymberknoh, M., Kerem, E., Avital, A., Springer, C., Hevroni, A. & Dabbah, H. & 14 others, Elizur, A., Picard, E., Goldberg, S., Rivlin, J., Livnat, G., Lavie, M., Alias, N., Soferman, R., Olbrich, H., Raidt, J., Wallmeier, J., Werner, C., Loges, N. T. & Omran, H., 1 Jan 2016, In: F1000Research. 5, 2031.
Research output: Contribution to journal › Article › peer-review

Open Access
5 Scopus citations
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practices
Abitbul, R., Amirav, I., Blau, H., Alkrinawi, S., Aviram, M., Shoseyov, D., Bentur, L., Avital, A., Springer, C., Lavie, M., Prais, D., Dabbah, H., Elias, N., Elizur, A., Goldberg, S., Hevroni, A., Kerem, E., Luder, A., Roth, Y. & Cohen-Cymberknoh, M. & 16 others, Ben Ami, M., Mandelberg, A., Livnat, G., Picard, E., Rivlin, J., Rotschild, M., Soferman, R., Loges, N. T., Olbrich, H., Werner, C., Wolter, A., Herting, M., Wallmeier, J., Raidt, J., Omran, H. & Mussaffi, H., 1 Oct 2016, In: Respiratory Medicine. 119, p. 41-47 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
12 Scopus citations
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis
and for the Israeli PCD Consortium Investigators, 1 Apr 2016, In: Human Mutation. 37, 4, p. 396-405 10 p.
Research output: Contribution to journal › Article › peer-review

Open Access
85 Scopus citations
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening
Stafler, P., Mei-Zahav, M., Wilschanski, M., Mussaffi, H., Efrati, O., Lavie, M., Shoseyov, D., Cohen-Cymberknoh, M., Gur, M., Bentur, L., Livnat, G., Aviram, M., Alkrinawi, S., Picard, E., Prais, D., Steuer, G., Inbar, O., Kerem, E. & Blau, H., 1 Jul 2016, In: Journal of Cystic Fibrosis. 15, 4, p. 460-466 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
33 Scopus citations
Essential role of carbonic anhydrase XII in secretory gland fluid and HCO₃^- secretion revealed by disease causing human mutation
Hong, J. H., Muhammad, E., Zheng, C., Hershkovitz, E., Alkrinawi, S., Loewenthal, N., Parvari, R. & Muallem, S., 15 Dec 2015, In: Journal of Physiology. 593, 24, p. 5299-5312 14 p.
Research output: Contribution to journal › Article › peer-review

Open Access
46 Scopus citations
Natural history and clinical manifestations of hyponatremia and hyperchlorhidrosis due to carbonic anhydrase XII deficiency
Feinstein, Y., Yerushalmi, B., Loewenthal, N., Alkrinawi, S., Birk, O. S., Parvari, R. & Hershkovitz, E., 1 Jan 2014, In: Hormone Research in Paediatrics. 81, 5, p. 336-342 7 p.
Research output: Contribution to journal › Article › peer-review
15 Scopus citations
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C
Romi, H., Cohen, I., Landau, D., Alkrinawi, S., Yerushalmi, B., Hershkovitz, R., Newman-Heiman, N., Cutting, G. R., Ofir, R., Sivan, S. & Birk, O. S., 4 May 2012, In: American Journal of Human Genetics. 90, 5, p. 893-899 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
86 Scopus citations

Soliman Alkrinawi

Personal profile

Fingerprint

Research output