-
1
-
2“…Goldberg polyhedra have been widely studied across multiple fields, as their distinctive pattern can lead to many useful applications. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
3por Takano, Hiromitsu, Yonezawa, Ikuho, Okuda, Takatoshi, Kajihara, Hajime, Kaneko, Kazuo“…We report a case of scoliosis in a 12-year-old girl with Shprintzen–Goldberg syndrome. She was diagnosed with Shprintzen–Goldberg syndrome at birth. …”
Publicado 2020
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
4por Rock, Kenneth L.Enlace del recurso
Publicado 2023
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
5“…Shprintzen-Goldberg Syndrome is an extremely infrequent disorder of connective tissue, characterized by craniosynostosis and marfanoid features, also known as Marfanoid Craniosynostosis syndrome. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
6“…Besides reproducing exotic structures such as M(30)L(60) and M(48)L(96) tetravalent Goldberg polyhedra, we identify highly cooperative single transition state rearrangements between low-energy competing structures as well, corresponding to rotatory motions of a planar subunit within the spherical shell.…”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
7por Beeby, MorganEnlace del recurso
Publicado 2019
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
8“…Goldberg's GHQ was translated into Hindi. An emphasis was made to have the language of common use. …”
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
9Psychometric Properties of The Goldberg Anxiety and Depression Scale (GADS) In Ecuadorian Population“…The objective of the present study was to analyze the psychometric properties of validity and reliability of the Goldberg Anxiety and Depression Scale (GADS) in Ecuadorian university students, since a cultural validation of the instrument has not been found in Ecuador. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10por MacKenzie, Katherine C., de Graaf, Bianca M., Syrimis, Andreas, Zhao, Yuying, Brosens, Erwin, Mancini, Grazia M. S., Schot, Rachel, Halley, Dicky, Wilke, Martina, Vøllo, Arve, Flinter, Frances, Green, Andrew, Mansour, Sahar, Pilch, Jacek, Stark, Zornitza, Zamba‐Papanicolaou, Eleni, Christophidou‐Anastasiadou, Violetta, Hofstra, Robert M. W., Jongbloed, Jan D. H., Nicolaou, Nayia, Tanteles, George A., Brooks, Alice S., Alves, Maria M.“…Goldberg–Shprintzen syndrome (GOSHS) is caused by loss of function variants in the kinesin binding protein gene (KIFBP). …”
Publicado 2020
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
11por SALEHPOUR, Shadab, HASHEMI-GORJI, Feyzollah, SOLTANI, Ziba, GHAFOURI-FARD, Soudeh, MIRYOUNESI, Mohammad“…Goldberg-Shprintzen syndrome (OMIM 609460) (GOSHS) is an autosomal recessive multiple congenital anomaly syndrome distinguished by intellectual disability, microcephaly, and dysmorphic facial characteristics. …”
Publicado 2017
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
12por Frank, John W.Enlace del recurso
Publicado 2022
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
13por Huxley, Peter, Krayer, Anne, Poole, Rob, Gromadzka, Alicja, Jie, Daniel Lai, Nafees, Sadia“…The first description of this ‘pathway’ to care and its levels and filters was published by Goldberg and Huxley in 1980. AIMS: To conduct a review of papers relevant to the application of the Goldberg–Huxley model in the 21st century. …”
Publicado 2023
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
14por Doyle, Alexander J., Doyle, Jefferson J., Bessling, Seneca L., Maragh, Samantha, Lindsay, Mark E., Schepers, Dorien, Gillis, Elisabeth, Mortier, Geert, Homfray, Tessa, Sauls, Kimberly, Norris, Russell A., Huso, Nicholas D., Leahy, Dan, Mohr, David W., Caulfield, Mark J., Scott, Alan F., Destrée, Anne, Hennekam, Raoul C., Arn, Pamela H., Curry, Cynthia J., Van Laer, Lut, McCallion, Andrew S., Loeys, Bart L., Dietz, Harry C.“…Taken together, these data have engendered controversy regarding the specific role of TGF-β in disease pathogenesis. Shprintzen-Goldberg syndrome (SGS) has considerable phenotypic overlap with MFS and LDS, including aortic aneurysm(6-8). …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
15“…Autosomal recessive mutations in KIAA1279 cause a rare neurological disorder, Goldberg-Shprintzen syndrome (GOSHS), characterized by microcephaly, polymicrogyria, intellectual disability, axonal neuropathy, thin corpus callosum and peripheral neuropathy. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
16
-
17por Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.“…Shprintzen–Goldberg craniosynostosis syndrome (SGS) is a rare autosomal dominant condition that was first documented in literature in 1982. …”
Publicado 2020
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
18“…The level of radiographic bony union (Goldberg method) was assessed by three orthopedic surgeons. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
19
-
20