Zobrazeno 1 - 10
of 2 065
pro vyhledávání: '"PETERLIN, B."'
Autor:
Siego, Cynthia Veronica, Sanchez, Sixto E., Jimenez, Maria L., Rondon, Marta B., Williams, Michelle A., Peterlin, B. Lee, Gelaye, Bizu
Publikováno v:
Universidad Peruana de Ciencias Aplicadas (UPC)Repositorio Academico - UPCJournal of Psychosomatic Research.
El texto completo de este trabajo no está disponible en el Repositorio Académico UPC por restricciones de la casa editorial donde ha sido publicado.
Objective: The objective of this study was to evaluate the association between (1) different t
Objective: The objective of this study was to evaluate the association between (1) different t
Externí odkaz:
http://hdl.handle.net/10757/658640
Autor:
Friedman, Lauren E., Aponte, Christina, Perez Hernandez, Rigoberto, Velez, Juan Carlos, Gelaye, Bizu, Sánchez, Sixto E., Williams, Michelle A., Peterlin, B. Lee
Background Individually both migraine and post-traumatic stress disorder (PTSD) prevalence estimates are higher among women. However, there is limited data on the association of migraine and PTSD in women during pregnancy. Methods We examined the ass
Externí odkaz:
http://hdl.handle.net/10757/622191
http://repositorioacademico.upc.edu.pe/upc/handle/10757/622191
http://repositorioacademico.upc.edu.pe/upc/handle/10757/622191
Autor:
Peterlin, B. Lee1,2 (AUTHOR), Bond, Dale S.3 (AUTHOR), Ailani, Jessica4 (AUTHOR), Dodick, David W.5,6 (AUTHOR), Liu, Yingyi7 (AUTHOR), De Abreu Ferreira, Rosa7 (AUTHOR), Smith, Jonathan H.7 (AUTHOR), Dabruzzo, Brett7 (AUTHOR) brett.dabruzzo@abbvie.com, Goadsby, Peter J.8,9 (AUTHOR), Trugman, Joel M.7 (AUTHOR)
Publikováno v:
Cephalalgia. Dec2024, Vol. 44 Issue 12, p1-11. 11p.
Autor:
Volk M, Writzl K, Veble A, Jaklič H, Teran N, Prosenc B, Štimpfel M, Virant Klun I, Vrtačnik Bokal E, Ban Frangež H, Peterlin B
Publikováno v:
Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 5-10 (2024)
Preimplantation genetic testing (PGT) is the earliest form of prenatal diagnosis that has become an established procedure for couples at risk of passing a severe genetic disease to their offspring. At UMC Ljubljana, we conducted a retrospective regis
Externí odkaz:
https://doaj.org/article/6c96e592e7ff4b3d998ebf6d0eaa66d8
Autor:
Sarajlija A., Armengol L., Maver A., Kitic I., Prokic D., Cehic M., Djuricic M.S., Peterlin B.
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 1, Pp 93-100 (2023)
Deficiency of lysosomal acid lipase (LAL-D) is caused by biallelic pathogenic variants in the LIPA gene. Spectrum of LAL-D ranges from early onset of hepatosplenomegaly and psychomotor regression (Wolman disease) to a more chronic course (cholesteryl
Externí odkaz:
https://doaj.org/article/625562bf626b47c18182937dd6ebe100
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 1, Pp 85-88 (2023)
Heterozygous pathogenic and likely pathogenic sequence variants in the RUNX1 (Runt-related Transcription Factor 1) gene are a common genetic cause of decreased platelet count and/or platelet dysfunction and an increased risk of developing myelodyspla
Externí odkaz:
https://doaj.org/article/cdd72d9999014fe88189ecc459fca314
Publikováno v:
In Molecular Cell 2 February 2023 83(3):393-403
Autor:
Rogac M, Neubauer D, Leonardis L, Pecaric N, Meznaric M, Maver A, Sperl W, Garavaglia BM, Lamantea E, Peterlin B
Publikováno v:
Balkan Journal of Medical Genetics, Vol 24, Iss 2, Pp 5-14 (2022)
The goal of the study was to retrospectively evaluate a cohort of children and adults with mitochondrial diseases (MDs) in a single-center experience. Neurological clinical examination, brain magnetic resonance imaging (MRI) and spectroscopy, muscle
Externí odkaz:
https://doaj.org/article/285c4e26ee0b411688311fb7e252d1ce
Autor:
Chai, Qingqing, Li, Sunan, Collins, Morgan K., Li, Rongrong, Ahmad, Iqbal, Johnson, Silas F., Frabutt, Dylan A., Yang, Zhichang, Shen, Xiaojing, Sun, Liangliang, Hu, Jian, Hultquist, Judd F., Peterlin, B. Matija, Zheng, Yong-Hui
Publikováno v:
In Cell Reports 10 August 2021 36(6)
Publikováno v:
Balkan Journal of Medical Genetics, Vol 22, Iss 2, Pp 65-68 (2019)
Microcephaly is characterized by significant clinical and genetic heterogeneity, therefore reaching the genetic diagnosis remains challenging in this group of disorders. We describe a case of a girl with secondary microcephaly, associated with severe
Externí odkaz:
https://doaj.org/article/186768aefc7b48a78481e0de037c205a