Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Stephen F. Miller"'
Lung cyst and multinodular thyroid goiter: Keys to DICER1 syndrome diagnosis in a 16‐year‐old female
Autor:
James D. Tutor, Stephen F. Miller, Hiba Al Zubeidi, Anthony Sheyn, Jie Zhang, Regan Williams, Rose B. McGee
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2373-2376 (2020)
Abstract Pulmonary cysts and neoplasms, especially congenital or occurring at a young age, should be thoroughly investigated. Evaluation for DICER1 mutations should be performed if there is a family history of this syndrome, the lung cyst/neoplasm is
Externí odkaz:
https://doaj.org/article/3781273266c04c89801c7e7f5cd17bb9
Autor:
Sirwa Padash, Haron Obaid, Robert D. E. Henderson, Yaseen Padash, Scott J. Adams, Stephen F. Miller, Paul Babyn
Publikováno v:
Pediatric Radiology. 53:971-983
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecda0c2a96128015dd2d79d860e6a3cd
https://doi.org/10.1007/s00247-022-05585-3
https://doi.org/10.1007/s00247-022-05585-3
Lung cyst and multinodular thyroid goiter: Keys to DICER1 syndrome diagnosis in a 16‐year‐old female
Autor:
Rose B. McGee, Anthony Sheyn, Hiba Al Zubeidi, Stephen F. Miller, James D. Tutor, Jie Zhang, Regan F. Williams
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2373-2376 (2020)
Clinical Case Reports
Clinical Case Reports
Pulmonary cysts and neoplasms, especially congenital or occurring at a young age, should be thoroughly investigated. Evaluation for DICER1 mutations should be performed if there is a family history of this syndrome, the lung cyst/neoplasm is a pleuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c909689d857879a4297ac522c8f37fab
https://doi.org/10.1002/ccr3.3098
https://doi.org/10.1002/ccr3.3098
Publikováno v:
Radiographics : a review publication of the Radiological Society of North America, Inc. 37(3)
The most important clues to narrow differential diagnosis of benign bone tumors in the pediatric population include patient age, location of the lesion, number of lesions, type of matrix, margin features, and presence of periosteal reaction and extra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb9f1a5b2d76041f284f2208e7dcfcb1
https://pubmed.ncbi.nlm.nih.gov/28493806
https://pubmed.ncbi.nlm.nih.gov/28493806
Autor:
Eniko K. Pivnick, Ahmad Khalid, Jewell C. Ward, Henry Joel Mroczkowski, Stephen F. Miller, Roya Mostafavi
Publikováno v:
American Journal of Obstetrics and Gynecology. 218:S171-S172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c303d9a328c7cd7283f7462585f8778
https://doi.org/10.1016/j.ajog.2017.10.198
https://doi.org/10.1016/j.ajog.2017.10.198
Autor:
Stephen F. Miller
Publikováno v:
Pediatric Radiology. 44:56-63
Juxtacortical chondroma is a rare benign bone lesion in children. Children usually present with a mildly painful mass, which prompts diagnostic imaging studies. The rarity of this condition often presents a diagnostic challenge. Correct diagnosis is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51c600d6956321dc9ac6d94e77804f7c
https://doi.org/10.1007/s00247-013-2770-6
https://doi.org/10.1007/s00247-013-2770-6
Publikováno v:
Pediatric Radiology. 40:747-761
Most of the common skeletal dysplasias have some manifestation in the hand. Many have characteristic findings in the hand that lead to the diagnosis. Hand bones are also affected in many systemic hematologic and metabolic conditions. The diagnosis ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c38afb3089fd196238358d472b42afe
https://doi.org/10.1007/s00247-009-1520-2
https://doi.org/10.1007/s00247-009-1520-2
Publikováno v:
Clinical Dysmorphology. 18:160-163
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ffa522e1434d3d1814a2d6c4b17efb
https://doi.org/10.1097/mcd.0b013e32832b44e1
https://doi.org/10.1097/mcd.0b013e32832b44e1
Autor:
Teresa Costa, Ants Toi, Sarah Keating, Dina J. Zand, Elaine H. Zackai, Earl D. Silverman, Sheila Unger, George E. Tiller, John Kingdom, David Chitayat, Cynthia J. Curry, Stephen F. Miller
Publikováno v:
American Journal of Medical Genetics Part A. :3038-3053
Chondrodysplasia punctata (CDP) is etiologically a heterogeneous condition and has been associated with single gene disorders, chromosome abnormalities and teratogenic exposures. The first publication of the association between CDP and maternal autoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab9fe67aa69c5c3028fca1ce4b105b56
https://doi.org/10.1002/ajmg.a.32554
https://doi.org/10.1002/ajmg.a.32554
Autor:
Susan Blaser, Sarah Keating, Ants Toi, Stephen F. Miller, Megan Thompson, Karen Chong, Elka Miller, Sheila Unger, Howard Berger
Publikováno v:
Pediatric Radiology. 38:1345-1349
The diastrophic dysplasia family of osteochondrodysplasias comprises a spectrum of skeletal diseases characterized by abnormal growth and remodelling of cartilage and bone. They are caused by mutations in the diastrophic dysplasia sulfate transporter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f2b35361365eab77e42b8f0b1a17ffb
https://doi.org/10.1007/s00247-008-0974-y
https://doi.org/10.1007/s00247-008-0974-y