Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Claudia M. Salgado"'
Autor:
Mylarappa Ningappa, Morayooluwa Adenuga, Kim A. Ngo, Nada Mohamed, Tejaswini Narayanan, Krishna Prasadan, Chethan Ashokkumar, Jishnu Das, Lori Schmitt, Hannah Hartman, Anuradha Sehrawat, Claudia M. Salgado, Miguel Reyes-Mugica, George K. Gittes, Cecilia W. Lo, Shankar Subramaniam, Rakesh Sindhi
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
BackgroundCiliary defects cause heterogenous phenotypes related to mutation burden which lead to impaired development. A previously reported homozygous deletion in the Man1a2 gene causes lethal respiratory failure in newborn pups and decreased lung c
Externí odkaz:
https://doaj.org/article/3f4d7397ddc74908a9f0fca602f5c229
Autor:
Vikrant Sood, Eliza J. Lee, Vikram Raghu, Miguel Reyes‐Mugica, Claudia M. Salgado, James Squires, George Mazariegos
Publikováno v:
Pediatric Transplantation. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3e9c427dec1890d46eef3a782993f7
https://doi.org/10.1111/petr.14488
https://doi.org/10.1111/petr.14488
Autor:
Jessica Daley, Katharine Halligan, Denise Howrie, Claudia M. Salgado, Alexandra Superdock, Erika Friehling, Kelly M. Bailey
Publikováno v:
Journal of Pediatric Hematology/Oncology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5188f0d8a8c6e5f2232d8e76d05e8078
https://doi.org/10.1097/mph.0000000000002623
https://doi.org/10.1097/mph.0000000000002623
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
17q12 deletion syndrome causes developmental abnormalities of the kidneys, pancreas, genital tract, and neurodevelopment, and it has a wide range of phenotypes ranging from fetal demise to normal adulthood with minimal renal impairment. Here we descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9805e31275876960e77b2276016d821c
https://pubmed.ncbi.nlm.nih.gov/36513606
https://pubmed.ncbi.nlm.nih.gov/36513606
Autor:
Shaymaa Hegazy, Mariana C. Marques, Scott W. Canna, Raphaela Goldbach-Mansky, Adriana A. de Jesus, Miguel Reyes-Múgica, Claudia M. Salgado
Publikováno v:
Am J Dermatopathol
A 15 - month-old full-term male of African descent with an asymptomatic sickle cell trait, presented with episodes of transient erythematous subcutaneous nodules involving the entire body except the face, since 2 weeks of age. The skin lesions evolve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d038383287728321ebf1c858def3fd26
https://europepmc.org/articles/PMC9117406/
https://europepmc.org/articles/PMC9117406/
Autor:
Claudia M. Salgado, Rita Alaggio, Andrea Ciolfi, Angelica Zin, Francesca Diomedi Camassei, Lucia Pedace, Giuseppe Maria Milano, Annalisa Serra, Angela Di Giannatale, Angela Mastronuzzi, Andrea Gianatti, Gianni Bisogno, Andrea Ferrari, Marco Tartaglia, Miguel Reyes-Múgica, Franco Locatelli, Evelina Miele
Publikováno v:
Modern Pathology. 36:100039
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cc77ea967ec24434e5af990ba09370e
https://doi.org/10.1016/j.modpat.2022.100039
https://doi.org/10.1016/j.modpat.2022.100039
Autor:
Jessica Daley, Nathan Williams, Claudia M. Salgado, Charles Schultz, Julia Meade, John Ozolek, Brock Lindsey, Kelly M. Bailey
Publikováno v:
Journal of pediatric hematology/oncology. 44(8)
Ewing sarcoma is an EWS-ETS family member-driven malignancy that most commonly arises from bone. Cutaneous Ewing sarcoma is a rare variant which harbors an EWS-ETS family fusion but demonstrates an immunohistochemical staining pattern distinct from c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73e7206dc522a0cb52245a10ac07c91
https://pubmed.ncbi.nlm.nih.gov/35426856
https://pubmed.ncbi.nlm.nih.gov/35426856
Autor:
Marti Goldenberg, Archana (AR) Ramgopal, Cláudia M. Salgado, Miguel Reyes‐Múgica, Marcus M. Malek, Jean M. Tersak
Publikováno v:
Cancer Reports, Vol 5, Iss 1, Pp n/a-n/a (2022)
Abstract Background Mesenchymal chondrosarcoma is a rare and aggressive bone tumor with few reports of primary tumor in the chest wall. Case We report a case of a 17‐year‐old male presenting with back pain and a posterior mediastinal mass. Imagin
Externí odkaz:
https://doaj.org/article/64c6033121c74fa99992d6e046e52f6f
Autor:
Dipanjan Basu, Cláudia M. Salgado, Janki R. Patel, Joie Zabec, Ryan M. Hoehl, Bruce Bauer, Miguel Reyes-Múgica
Publikováno v:
Biomarker Research, Vol 7, Iss 1, Pp 1-5 (2019)
Abstract Factors regulating transcription of pluripotency genes in congenital nevo-melanocytes are not known. Nevo-melanocytes belong somewhere in-between the ends of a spectrum where the normal epidermal melanocyte represents one end and a melanoma
Externí odkaz:
https://doaj.org/article/de0b5f2d11e440d4ba2dd9831123d79d