Search Results - "Marfan syndrome"

Primary Diagnosis of Marfan Syndrome in Pregnant 16 Years Old Girl: a Clinical Case by Evgeniy S. Mikhaylin, Lada A. Ivanova, Mariya M. Shilo

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TGFβ level in healthy and children with Marfan syndrome-effective reduction under sartan therapy by Veronika C. Stark, Jakob Olfe, Daniel Diaz-Gil, Daniel Diaz-Gil, Yskert von Kodolitsch, Rainer Kozlik-Feldmann, Johannes Reincke, Maria Stark, Peter Wiegand, Tanja Zeller, Tanja Zeller, Thomas S. Mir

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PREGNANCY AND DELIVERY IN PATIENTS WITH MESENHYMAL DYSPLASIAS (MARFAN SYNDROME, EHLERS-DANLOS SYNDROME, HEREDITARY HEMORRHAGIC TELANGIECTASIA) by L. S. Radetskaya, A. D. Makatsariya

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Genetically engineered animal models for Marfan syndrome: challenges associated with the generation of pig models for diseases caused by haploinsufficiency by Naomi JACK, Tomoyuki MUTO, Keigo IEMITSU, Tamaki WATANABE, Kazuhiro UMEYAMA, Jun OHGANE, Hiroshi NAGASHIMA

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Marfan syndrome in childhood: parents' perspectives of the impact on daily functioning of children, parents and family; a qualitative study by Jessica Warnink-Kavelaars, Anita Beelen, Sarah Dekker, Frans Nollet, Leonie A. Menke, Raoul H. H. Engelbert

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Application of cook balloon during aorta replacement in a pregnant Marfan-syndrome patient: a case report by Lu Zhang, Bin Yan, Xue Cui, Jinghong Liu, Fangxin Shi

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Gelatinolytic activity in gingival crevicular fluid and saliva of growing patients with Marfan syndrome: a case-control study by Giuseppina Laganà, Giovanni Francesco Fasciglione, Andrea Biondi, Massimiliano Coletta, Giovanni Ruvolo, Paola Cozza

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PREGNANCY AND HERITABLE CONNECTIVE TISSUE DISORDERS (MARFAN SYNDROME, EHLERS DANLOS SYNDROME, OSLER-WEBER-RENDU DISEASE) by L. S. Radetskaya

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Targeted deletion of fibrillin-1 in the mouse eye results in ectopia lentis and other ocular phenotypes associated with Marfan syndrome by Wendell Jones, Juan Rodriguez, Steven Bassnett

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A case series describing the risk of periodontal disease in Marfan syndrome patients harboring a possible aortic aneurysm or dissection by Kouta Umezawa, Takako Kajiwara, Kyoko Ishii, Tatsuya Hasegawa, Shigeto Suzuki, Masato Nakano, Mayu Sawaguchi, Venkata Suresh Venkataiah, Yoshio Yahata, Koki Ito, Yoshikatsu Saiki, Masahiro Saito

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A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report by Yuping Niu, Sexin Huang, Zeyu Wang, Peiwen Xu, Lijuan Wang, Jie Li, Ming Gao, Xuan Gao, Yuan Gao

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Mutation in Genes FBN1, AKT1, and LMNA: Marfan Syndrome, Proteus Syndrome, and Progeria Share Common Systemic Involvement by Tonmoy Biswas

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Acute type B aortic dissection in a pregnant woman with undiagnosed Marfan syndrome: A case report and review of the literature by Yumiko Miyazaki, Makoto Orisaka, Masataka Kato, Hiroshi Kawamura, Tetsuji Kurokawa, Yoshio Yoshida

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Neonatal Marfan syndrome: a case report of a novel fibrillin 1 mutation, with genotype-phenotype correlation and brief review of the literature by Flaminia Pugnaloni, Domenico Umberto De Rose, Maria Cristina Digilio, Monia Magliozzi, Annabella Braguglia, Laura Valfrè, Alessandra Toscano, Andrea Dotta, Alessandra Di Pede

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Fibrillin-1 mutation contributes to Marfan syndrome by inhibiting Cav1.2-mediated cell proliferation in vascular smooth muscle cells by Wenfeng Lin, Jiaqi Xiong, Yefan Jiang, Hao Liu, Jinhui Bian, Juejin Wang, Yongfeng Shao, Buqing Ni

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Orthodontic-surgical treatment of a patient with Marfan Syndrome and Obstructive Sleep Apnea Syndrome: a case report with a 9-year follow-up by Willian Caetano RODRIGUES, Mário Francisco Real GABRIELLI, Marina Reis OLIVEIRA, Ana Cláudia Gabrielli PIVETA, Marisa Aparecida Cabrini GABRIELLI

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Successful Kidney Transplantation in a Patient with Marfan's Syndrome with a History of Aortic Dissection Operation and a Dissection Flap Up to the Iliac Bifurcation Level by Vural Taner Yılmaz, Abdullah Kısaoğlu, Ali Avanaz, İsmail Demiryılmaz, Fahri Uçar, Bülent Aydınlı, Hüseyin Koçak

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Updated 2022 ACC/AHA Guideline Improves Concordance Between TTE and CT in Monitoring Marfan Syndrome and Related Disorders, but Relevant Measurement Differences Remain Frequent by Johannes Kolck, Tobias Daniel Trippel, Karla Philipp, Petra Gehle, Dominik Geisel, Nick Lasse Beetz

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Manifestações Cardiovasculares em Paciente Portador de Síndrome de Marfan: Relato de Caso / Cardiovascular Manifestations in a Patient With Marfan's Syndrome: Case Report by Eduardo Tadeu Ramos Almeida, Fábio Sergio Ferreira Resende Fonseca, Flávia Sala Pasquinelli

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A 45-year-old Italian male with p.(Gly1815Ser) FBN1 mutation causing a mild variant of Marfan syndrome: A case study by Francesca Cortini, Chiara Villa, Barbara Marinelli, Sara Franchetti, Luciano Riboldi, Alessandra Bassotti

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