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Quoted phrase not found in phrase index: "Abnormal form of the vertebral bodies"
Page 1
Retinoid signaling in skeletal development: Scoping the system for predictive toxicology.
Knudsen TB, Pierro JD, Baker NC. Knudsen TB, et al. Reprod Toxicol. 2021 Jan;99:109-130. doi: 10.1016/j.reprotox.2020.10.014. Epub 2020 Nov 14. Reprod Toxicol. 2021. PMID: 33202217 Review.
All-trans retinoic acid (ATRA), the biologically active form of vitamin A, is instrumental in regulating the patterning and specification of the vertebrate embryo. ...Windows of vulnerability for altered skeletal patterning coincide with early specification of the body …
All-trans retinoic acid (ATRA), the biologically active form of vitamin A, is instrumental in regulating the patterning and specifica …
Multiple vertebral segmentation defects: analysis of 26 new patients and review of the literature.
Mortier GR, Lachman RS, Bocian M, Rimoin DL. Mortier GR, et al. Am J Med Genet. 1996 Feb 2;61(4):310-9. doi: 10.1002/(SICI)1096-8628(19960202)61:4<310::AID-AJMG3>3.0.CO;2-Y. Am J Med Genet. 1996. PMID: 8834041 Review.
Spondylothoracic dysostosis shows considerable clinical and radiographic overlap with spondylocostal dysostosis. Malformations observed in association with multiple vertebral segmentation defects are more common in the sporadic patients. Analysis of the 26 new indiv …
Spondylothoracic dysostosis shows considerable clinical and radiographic overlap with spondylocostal dysostosis. Malformations observed …
Paraxial mesoderm organoids model development of human somites.
Budjan C, Liu S, Ranga A, Gayen S, Pourquié O, Hormoz S. Budjan C, et al. Elife. 2022 Jan 28;11:e68925. doi: 10.7554/eLife.68925. Elife. 2022. PMID: 35088712 Free PMC article.
Although this is not very obvious in humans, vertebrate bodies are derived from pairs of segments arranged from the head to the tail. Each of these segments or somites originates early in embryonic development. Cells from each somite then divide, grow and specialize to …
Although this is not very obvious in humans, vertebrate bodies are derived from pairs of segments arranged from the head to the tail. …
The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention.
Ferreira CR, Regier DS, Yoon R, Pan KS, Johnston JM, Yang S, Spranger JW, Tifft CJ. Ferreira CR, et al. Bone. 2020 Feb;131:115142. doi: 10.1016/j.bone.2019.115142. Epub 2019 Nov 6. Bone. 2020. PMID: 31704340 Free PMC article.
All late infantile patients had odontoid hypoplasia and pear-shaped vertebral bodies, the frequency of which was significantly different than in patients with juvenile disease (none and 14%, respectively). Juvenile patients had irregular endplates of the vertebra …
All late infantile patients had odontoid hypoplasia and pear-shaped vertebral bodies, the frequency of which was significantly …
Micro-computed tomography assessment of vertebral column defects in retinoic acid-induced rat model of myelomeningocele.
Barbe MF, Adiga R, Gordiienko O, Pleshko N, Selzer ME, Krynska B. Barbe MF, et al. Birth Defects Res A Clin Mol Teratol. 2014 Jun;100(6):453-62. doi: 10.1002/bdra.23254. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24954432
RESULTS: We observed, in detail, skeletal defects in lumbosacral vertebra of MMC rats, including in the morphology of individual dorsal vertebral arches. Use of high resolution micro-CT has also enabled us to identify the delayed (nonfused) or absent ossification in …
RESULTS: We observed, in detail, skeletal defects in lumbosacral vertebra of MMC rats, including in the morphology of individual dors …
Cervical spine in the Apert syndrome.
Kreiborg S, Barr M Jr, Cohen MM Jr. Kreiborg S, et al. Am J Med Genet. 1992 Jul 1;43(4):704-8. doi: 10.1002/ajmg.1320430411. Am J Med Genet. 1992. PMID: 1621762
Autopsy material was available in one of these cases, and a 3-dimensional reconstruction from a CT scan was also studied in one case. Variable degrees of fusion were observed, involving the articular facets, the neural arch or transverse processes, or block fusion of the …
Autopsy material was available in one of these cases, and a 3-dimensional reconstruction from a CT scan was also studied in one case. Variab …
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new cases.
Bownass L, Abbs S, Armstrong R, Baujat G, Behzadi G, Berentsen RD, Burren C, Calder A, Cormier-Daire V, Newbury-Ecob R, Foulds N, Juliusson PB, Kant SG, Lefroy H, Mehta SG, Merckoll E, Michot C, Monsell F, Offiah AC, Richards A, Rosendahl K, Rustad CF, Shears D, Tveten K, Wellesley D, Wordsworth P; Deciphering Developmental Disorders Study; Smithson S. Bownass L, et al. Am J Med Genet A. 2019 Sep;179(9):1884-1894. doi: 10.1002/ajmg.a.61282. Epub 2019 Jul 16. Am J Med Genet A. 2019. PMID: 31313512 Free article.
Brachyolmia is a skeletal dysplasia characterized by short spine-short stature, platyspondyly, and minor long bone abnormalities. We describe 18 patients, from different ethnic backgrounds and ages ranging from infancy to 19 years, with the autosomal recessive form, …
Brachyolmia is a skeletal dysplasia characterized by short spine-short stature, platyspondyly, and minor long bone abnormalities. We …
Brachyolmia: radiographic and genetic evidence of heterogeneity.
Shohat M, Lachman R, Gruber HE, Rimoin DL. Shohat M, et al. Am J Med Genet. 1989 Jun;33(2):209-19. doi: 10.1002/ajmg.1320330214. Am J Med Genet. 1989. PMID: 2669482 Review.
Hobaek type--an autosomal recessive condition with universal platyspondyly, irregular, and reduced intervertebral spaces and marked extension of the lateral margins of the vertebrae. Rectangular and elongated vertebral bodies are seen on lateral views of the spine, …
Hobaek type--an autosomal recessive condition with universal platyspondyly, irregular, and reduced intervertebral spaces and marked extensio …
Symptomatic relevance of intravertebral cleft in patients with osteoporotic vertebral fracture.
Kawaguchi S, Horigome K, Yajima H, Oda T, Kii Y, Ida K, Yoshimoto M, Iba K, Takebayashi T, Yamashita T. Kawaguchi S, et al. J Neurosurg Spine. 2010 Aug;13(2):267-75. doi: 10.3171/2010.3.SPINE09364. J Neurosurg Spine. 2010. PMID: 20672965
The extent of dynamic mobility of the vertebra correlated significantly with the VAS score in patients with an unhealed OVF. In addition, a significant correlation with the extent of dynamic vertebral mobility with performance status was seen in patients with an unh …
The extent of dynamic mobility of the vertebra correlated significantly with the VAS score in patients with an unhealed OVF. In addit …
Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase Deficiency.
Atay Z, Turan S, Buğdaycı O, Guran T, Bereket A. Atay Z, et al. Horm Res Paediatr. 2019;92(3):203-208. doi: 10.1159/000501456. Epub 2019 Aug 27. Horm Res Paediatr. 2019. PMID: 31454824
11beta-hydroxylase deficiency (11beta-OHD) is the second most common form of congenital adrenal hyperplasia (CAH). Males with 11beta-OHD CAH are often diagnosed late with a significantly advanced bone age leading to a poor height prognosis due to early closure of ep …
11beta-hydroxylase deficiency (11beta-OHD) is the second most common form of congenital adrenal hyperplasia (CAH). Males with …
24 results