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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 2
1975 1
1976 2
1977 3
1978 4
1979 2
1980 3
1982 3
1983 3
1984 1
1985 1
1986 2
1987 2
1988 4
1989 3
1990 1
1991 8
1992 9
1993 6
1994 5
1995 5
1996 8
1997 7
1998 10
1999 8
2000 7
2001 7
2002 11
2003 14
2004 12
2005 14
2006 15
2007 11
2008 18
2009 17
2010 12
2011 15
2012 17
2013 25
2014 16
2015 25
2016 16
2017 16
2018 25
2019 22
2020 21
2021 23
2022 27
2023 24
2024 15

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472 results

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Quoted phrase not found in phrase index: "Abnormality of skeletal maturation"
Page 1
Epidemiology, Staging, and Management of Multiple Myeloma.
Padala SA, Barsouk A, Barsouk A, Rawla P, Vakiti A, Kolhe R, Kota V, Ajebo GH. Padala SA, et al. Med Sci (Basel). 2021 Jan 20;9(1):3. doi: 10.3390/medsci9010003. Med Sci (Basel). 2021. PMID: 33498356 Free PMC article. Review.
International staging system staging involves beta 2 microglobulin and albumin levels, while the revised system considers prognostic factors such as lactate dehydrogenase levels and chromosomal abnormalities. Front-line management includes induction regimen, maintenance th …
International staging system staging involves beta 2 microglobulin and albumin levels, while the revised system considers prognostic factors …
Blount disease.
Janoyer M. Janoyer M. Orthop Traumatol Surg Res. 2019 Feb;105(1S):S111-S121. doi: 10.1016/j.otsr.2018.01.009. Epub 2018 Feb 23. Orthop Traumatol Surg Res. 2019. PMID: 29481866 Free article. Review.
A consensus exists about the optimal treatment in two situations: before 4 years of age, progressive Blount disease should be corrected, preferably by a simple osteotomy; and once medial tibial epiphysiodesis has developed, both a complementary epiphysiodesis and gradual external …
A consensus exists about the optimal treatment in two situations: before 4 years of age, progressive Blount disease should be corrected, pre …
Congenital Titinopathy: Comprehensive characterization and pathogenic insights.
Oates EC, Jones KJ, Donkervoort S, Charlton A, Brammah S, Smith JE 3rd, Ware JS, Yau KS, Swanson LC, Whiffin N, Peduto AJ, Bournazos A, Waddell LB, Farrar MA, Sampaio HA, Teoh HL, Lamont PJ, Mowat D, Fitzsimons RB, Corbett AJ, Ryan MM, O'Grady GL, Sandaradura SA, Ghaoui R, Joshi H, Marshall JL, Nolan MA, Kaur S, Punetha J, Töpf A, Harris E, Bakshi M, Genetti CA, Marttila M, Werlauff U, Streichenberger N, Pestronk A, Mazanti I, Pinner JR, Vuillerot C, Grosmann C, Camacho A, Mohassel P, Leach ME, Foley AR, Bharucha-Goebel D, Collins J, Connolly AM, Gilbreath HR, Iannaccone ST, Castro D, Cummings BB, Webster RI, Lazaro L, Vissing J, Coppens S, Deconinck N, Luk HM, Thomas NH, Foulds NC, Illingworth MA, Ellard S, McLean CA, Phadke R, Ravenscroft G, Witting N, Hackman P, Richard I, Cooper ST, Kamsteeg EJ, Hoffman EP, Bushby K, Straub V, Udd B, Ferreiro A, North KN, Clarke NF, Lek M, Beggs AH, Bönnemann CG, MacArthur DG, Granzier H, Davis MR, Laing NG. Oates EC, et al. Ann Neurol. 2018 Jun;83(6):1105-1124. doi: 10.1002/ana.25241. Ann Neurol. 2018. PMID: 29691892 Free PMC article.
OBJECTIVE: Comprehensive clinical characterization of congenital titinopathy to facilitate diagnosis and management of this important emerging disorder. ...One-third of patients had 1 mutation predicted to impact exons present in fetal skeletal muscle, but not inclu …
OBJECTIVE: Comprehensive clinical characterization of congenital titinopathy to facilitate diagnosis and management of this important …
Hereditary inclusion-body myopathies.
Broccolini A, Mirabella M. Broccolini A, et al. Biochim Biophys Acta. 2015 Apr;1852(4):644-50. doi: 10.1016/j.bbadis.2014.08.007. Epub 2014 Aug 19. Biochim Biophys Acta. 2015. PMID: 25149037 Free article. Review.
The most common form of HIBM is due to mutations of the GNE gene that codes for a rate-limiting enzyme in the sialic acid biosynthetic pathway. This results in abnormal sialylation of glycoproteins that possibly leads to muscle fiber degeneration. Mutations of the valosin …
The most common form of HIBM is due to mutations of the GNE gene that codes for a rate-limiting enzyme in the sialic acid biosynthetic pathw …
Myeloma Bone Disease: A Comprehensive Review.
Mukkamalla SKR, Malipeddi D. Mukkamalla SKR, et al. Int J Mol Sci. 2021 Jun 8;22(12):6208. doi: 10.3390/ijms22126208. Int J Mol Sci. 2021. PMID: 34201396 Free PMC article. Review.
Osteolytic lesions are seen in 80% of patients with MM which are complicated frequently by skeletal-related events (SRE) such as hypercalcemia, bone pain, pathological fractures, vertebral collapse, and spinal cord compression. ...This review article summarizes the pathoph …
Osteolytic lesions are seen in 80% of patients with MM which are complicated frequently by skeletal-related events (SRE) such as hype …
Assessment of Skeletal Maturation in Nonsyndromic Cleft and Non-cleft Children-A Comparative Study.
Qureshi T, Kharbanda OP, Duggal R. Qureshi T, et al. J Craniofac Surg. 2023 Oct 1;34(7):1948-1952. doi: 10.1097/SCS.0000000000009356. Epub 2023 May 29. J Craniofac Surg. 2023. PMID: 37253236
The study aims to determine the difference in the skeletal maturation of unilateral cleft lip and palate (UCLP) and non-cleft children. ...There was no significant difference in the mean chronological age and skeletal maturation status of UCLP and non- …
The study aims to determine the difference in the skeletal maturation of unilateral cleft lip and palate (UCLP) and non-cleft …
Facial infiltrating lipomatosis.
Padwa BL, Mulliken JB. Padwa BL, et al. Plast Reconstr Surg. 2001 Nov;108(6):1544-54. doi: 10.1097/00006534-200111000-00017. Plast Reconstr Surg. 2001. PMID: 11711926
Facial infiltrating lipomatosis is a rare congenital disorder in which mature lipocytes invade adjacent tissue. The phenotypic features include soft-tissue and skeletal hypertrophy, premature dental eruption, and regional macrodontia. ...
Facial infiltrating lipomatosis is a rare congenital disorder in which mature lipocytes invade adjacent tissue. The phenotypic …
Sexual precocity and its treatment.
Brown DB, Loomba-Albrecht LA, Bremer AA. Brown DB, et al. World J Pediatr. 2013 May;9(2):103-11. doi: 10.1007/s12519-013-0411-7. Epub 2013 May 16. World J Pediatr. 2013. PMID: 23677828 Review.
Regardless of the etiology, sexual precocity causes increased height velocity, somatic development, and skeletal maturation, which may have profound physical and psychological implications. ...Alternatively, the treatment of disorders causing GnRH-independent sexual …
Regardless of the etiology, sexual precocity causes increased height velocity, somatic development, and skeletal maturation, w …
Skeletal Maturation in Patients With Cleft Lip and/or Palate: A Systematic Review.
Wu X, Kuang W, Zheng J, Yang Z, Ren M, Yang R, Yuan W. Wu X, et al. Cleft Palate Craniofac J. 2022 Mar;59(3):307-319. doi: 10.1177/10556656211007680. Epub 2021 Apr 8. Cleft Palate Craniofac J. 2022. PMID: 33827285
OBJECTIVE: The objective of this systematic review was to evaluate the evidence regarding skeletal maturation in patients with cleft lip and/or palate (CL/P) and to investigate whether the skeletal maturation is delayed in these patients. ...CONCLUSION …
OBJECTIVE: The objective of this systematic review was to evaluate the evidence regarding skeletal maturation in patients with …
Laminopathies: multisystem dystrophy syndromes.
Jacob KN, Garg A. Jacob KN, et al. Mol Genet Metab. 2006 Apr;87(4):289-302. doi: 10.1016/j.ymgme.2005.10.018. Epub 2005 Dec 20. Mol Genet Metab. 2006. PMID: 16364671 Review.
Laminopathies are a heterogeneous group of genetic disorders due to abnormalities in type A lamins and can manifest varied clinical features affecting many organs including the skeletal and cardiac muscle, adipose tissue, nervous system, cutaneous tissue, and bone. …
Laminopathies are a heterogeneous group of genetic disorders due to abnormalities in type A lamins and can manifest varied clinical f …
472 results