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Select item 37980641.

Management of Uterine Bleeding During Hematopoietic Stem Cell Transplantation

Stephanie E. Purisch, Dana Shanis, Christa Zerbe, Melissa Merideth, Jennifer Cuellar-Rodriguez, Pamela Stratton

Obstet Gynecol. Author manuscript; available in PMC 2013 Oct 17.

Published in final edited form as: Obstet Gynecol. 2013 Feb; 121(2 0 2 0 1): 424–427. doi: 10.1097/aog.0b013e318270ecd3

PMCID:: PMC3798064

Abstract Article PDF–32K

Select item 59023122.

Selective effects of oral anti-angiogenic tyrosine kinase inhibitors on an animal model of hereditary hemorrhagic telangiectasia

Yong Hwan Kim, Mi-Jung Kim, Se-woon Choe, Dennis Sprecher, Young Jae Lee, S. Paul Oh

J Thromb Haemost. Author manuscript; available in PMC 2018 Jun 1.

Published in final edited form as: J Thromb Haemost. 2017 Jun; 15(6): 1095–1102. Published online 2017 May 3. doi: 10.1111/jth.13683

PMCID:: PMC5902312

Abstract Article PDF–2.4M

Select item 58845123.

Loss of HAI-2 in mice with decreased prostasin activity leads to an early-onset intestinal failure resembling congenital tufting enteropathy

Roman Szabo, Thomas H. Bugge

PLoS One. 2018; 13(4): e0194660. Published online 2018 Apr 4. doi: 10.1371/journal.pone.0194660

PMCID:: PMC5884512

Abstract Article PDF–24M

Select item 57963644.

Hemorrhagic Brain Metastases in a Patient with Anaplastic Lymphoma Kinase (ALK)-Rearranged Invasive Mucinous Adenocarcinoma of the Lung

Mingxia Shi, Hongzhi Xu, Angela DiPoto Brahmbhatt, Eduardo Gonzalez-Toledo, Maria-Magdalena Georgescu

Am J Case Rep. 2018; 19: 99–104. Published online 2018 Jan 26. doi: 10.12659/AJCR.906803

PMCID:: PMC5796364

Abstract Article PDF–2.3M

Select item 54117395.

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca²⁺ homeostasis and ER-mitochondria interactions

Cécile Rouzier, David Moore, Cécile Delorme, Sandra Lacas-Gervais, Samira Ait-El-Mkadem, Konstantina Fragaki, Florence Burté, Valérie Serre, Sylvie Bannwarth, Annabelle Chaussenot, Martin Catala, Patrick Yu-Wai-Man, Véronique Paquis-Flucklinger

Hum Mol Genet. 2017 May 1; 26(9): 1599–1611. Published online 2017 Mar 6. doi: 10.1093/hmg/ddx060

Correction in:: Hum Mol Genet. 2017 May 1; 26(9): 1786.

PMCID:: PMC5411739

Abstract Article PDF–1.2M

Select item 49434606.

Activation-Resistant Homozygous Protein C R229W Mutation Causing Familial Perinatal Intracranial Hemorrhage and Delayed Onset of Thrombosis

Abdulrahman Alsultan, Andrew J. Gale, Kadijah Kurban, Mohammed Khalifah, Fahad B. Albadr, John H. Griffin

Thromb Res. Author manuscript; available in PMC 2017 Jul 1.

Published in final edited form as: Thromb Res. 2016 Jul; 143: 17–21. Published online 2016 Apr 23. doi: 10.1016/j.thromres.2016.04.011

PMCID:: PMC4943460

Abstract Article PDF–1.3M

Select item 42757597.

Familial perimesencephalic subarachnoid hemorrhage: two case reports

Ulaş Cıkla, Beverly Aagaard-Kienitz, Patrick A Turski, Guner Menekse, David B Niemann, Mustafa K Başkaya

J Med Case Rep. 2014; 8: 380. Published online 2014 Nov 22. doi: 10.1186/1752-1947-8-380

PMCID:: PMC4275759

Abstract Article PDF–3.0M

Select item 42677738.

Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing

Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, Gregory Papagregoriou, Isavella Savva, Christoforos Stavrou, Michael Zavros, Yiannis Athanasiou, Kyriakos Ioannou, Charalambos Patsias, Alexia Panagides, Costas Potamitis, Kyproula Demetriou, Marios Prikis, Michael Hadjigavriel, Maria Kkolou, Panayiota Loukaidou, Androulla Pastelli, Aristos Michael, Akis Lazarou, Maria Arsali, Loukas Damianou, Ioanna Goutziamani, Andreas Soloukides, Lakis Yioukas, Avraam Elia, Ioanna Zouvani, Polycarpos Polycarpou, Alkis Pierides, Konstantinos Voskarides, Constantinos Deltas

PLoS One. 2014; 9(12): e115015. Published online 2014 Dec 16. doi: 10.1371/journal.pone.0115015

PMCID:: PMC4267773

Abstract Article PDF–726K

Select item 41620989.

Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease

Meral Gunay–Aygun, Esperanza Font–Montgomery, Linda Lukose, Maya Tuchman Gerstein, Katie Piwnica–Worms, Peter Choyke, Kailash T. Daryanani, Baris Turkbey, Roxanne Fischer, Isa Bernardini, Murat Sincan, Xiongce Zhao, Netanya G. Sandler, Annelys Roque, Daniel C. Douek, Jennifer Graf, Marjan Huizing, Joy C. Bryant, Parvathi Mohan, William A. Gahl, Theo Heller

Gastroenterology. Author manuscript; available in PMC 2014 Sep 12.

Published in final edited form as: Gastroenterology. 2013 Jan; 144(1): 112–121.e2. Published online 2012 Oct 3. doi: 10.1053/j.gastro.2012.09.056

PMCID:: PMC4162098

Abstract Article PDF–1.5M

Select item 411725610.

Absence of Association of Interleukin-18 Gene Polymorphisms with Primary Immune Thrombocytopenia in a Chinese Han Population

Huiyuan Li, Min Xuan, Feng Xue, Xiaofan Liu, Donglei Zhang, Rongfeng Fu, Yanhui Yang, Xian Zhang, Renchi Yang

DNA Cell Biol. 2014 Aug 1; 33(8): 537–542. doi: 10.1089/dna.2013.2247

PMCID:: PMC4117256

Abstract Article PDF–128K

Select item 399515811.

Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation

Hélène Choquet, Jeffrey Nelson, Ludmila Pawlikowska, Charles E. McCulloch, Amy Akers, Beth Baca, Yasir Khan, Blaine Hart, Leslie Morrison, Helen Kim

Cerebrovasc Dis. Author manuscript; available in PMC 2015 Jan 1.

Published in final edited form as: Cerebrovasc Dis. 2014; 37(1): 57–63. Published online 2013 Dec 21. doi: 10.1159/000356839

PMCID:: PMC3995158

Abstract Article PDF–52K

Select item 632912312.

Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report

Jun Ishihara, Tatsuki Mizuochi, Takashi Uchida, Yugo Takaki, Ken-ichiro Konishi, Masahiko Joo, Yasuhiko Takahashi, Shinichiro Yoshioka, Hironori Kusano, Yoji Sasahara, Yushiro Yamashita

BMC Gastroenterol. 2019; 19: 9. Published online 2019 Jan 11. doi: 10.1186/s12876-019-0929-9

PMCID:: PMC6329123

Abstract Article PDF–4.0M

Select item 372981713.

Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report

Koki Mise, Yoshifumi Ubara, Masanori Matsumoto, Keiichi Sumida, Rikako Hiramatsu, Eiko Hasegawa, Masayuki Yamanouchi, Noriko Hayami, Tatsuya Suwabe, Junichi Hoshino, Naoki Sawa, Kenichi Ohashi, Koichi Kokame, Toshiyuki Miyata, Yoshihiro Fujimura, Kenmei Takaichi

BMC Nephrol. 2013; 14: 156. Published online 2013 Jul 20. doi: 10.1186/1471-2369-14-156

PMCID:: PMC3729817

Abstract Article PDF–1.1M

Select item 366910314.

Expression of the Growth Factor Progranulin in Endothelial Cells Influences Growth and Development of Blood Vessels: A Novel Mouse Model

Huishi Toh, Mingju Cao, Eugene Daniels, Andrew Bateman

PLoS One. 2013; 8(5): e64989. Published online 2013 May 31. doi: 10.1371/journal.pone.0064989

PMCID:: PMC3669103

Abstract Article PDF–41M

Select item 330919415.

Mutations in CTC1, Encoding the CTS Telomere Maintenance Complex Component 1, Cause Cerebroretinal Microangiopathy with Calcifications and Cysts

Anne Polvi, Tarja Linnankivi, Tero Kivelä, Riitta Herva, James P. Keating, Outi Mäkitie, Davide Pareyson, Leena Vainionpää, Jenni Lahtinen, Iiris Hovatta, Helena Pihko, Anna-Elina Lehesjoki

Am J Hum Genet. 2012 Mar 9; 90(3): 540–549. doi: 10.1016/j.ajhg.2012.02.002