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

Year Number of Results
1968 1
1970 1
1972 1
1975 1
1976 1
1977 1
1978 1
1979 1
1980 2
1982 1
1983 1
1985 1
1986 2
1987 3
1990 2
1991 2
1993 1
1994 2
1995 1
1996 3
1997 3
1998 4
1999 1
2001 2
2002 3
2003 3
2004 2
2005 3
2006 4
2007 3
2008 6
2009 5
2010 5
2011 4
2012 4
2013 2
2014 4
2015 5
2016 6
2017 9
2018 12
2019 13
2020 7
2021 3
2022 2
2023 4
2024 0

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137 results

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Page 1
Chronic Kidney Disease Diagnosis and Management: A Review.
Chen TK, Knicely DH, Grams ME. Chen TK, et al. JAMA. 2019 Oct 1;322(13):1294-1304. doi: 10.1001/jama.2019.14745. JAMA. 2019. PMID: 31573641 Free PMC article. Review.
Patients also require monitoring for complications of CKD, such as hyperkalemia, metabolic acidosis, hyperphosphatemia, vitamin D deficiency, secondary hyperparathyroidism, and anemia. ...CONCLUSIONS AND RELEVANCE: Diagnosis, staging, and appropriate referral …
Patients also require monitoring for complications of CKD, such as hyperkalemia, metabolic acidosis, hyperphosphatemia, vitamin …
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.
Haffner D, Emma F, Eastwood DM, Duplan MB, Bacchetta J, Schnabel D, Wicart P, Bockenhauer D, Santos F, Levtchenko E, Harvengt P, Kirchhoff M, Di Rocco F, Chaussain C, Brandi ML, Savendahl L, Briot K, Kamenicky P, Rejnmark L, Linglart A. Haffner D, et al. Nat Rev Nephrol. 2019 Jul;15(7):435-455. doi: 10.1038/s41581-019-0152-5. Nat Rev Nephrol. 2019. PMID: 31068690 Free PMC article.
In this Evidence-Based Guideline, we recommend that the diagnosis of XLH is based on signs of rickets and/or osteomalacia in association with hypophosphataemia and renal phosphate wasting in the absence of vitamin D or calcium deficiency. Whenever possible, the diag …
In this Evidence-Based Guideline, we recommend that the diagnosis of XLH is based on signs of rickets and/or osteomalacia in association wit …
Management and prevention of bone stress injuries in long-distance runners.
Warden SJ, Davis IS, Fredericson M. Warden SJ, et al. J Orthop Sports Phys Ther. 2014 Oct;44(10):749-65. doi: 10.2519/jospt.2014.5334. Epub 2014 Aug 7. J Orthop Sports Phys Ther. 2014. PMID: 25103133
The former is more amenable to intervention and may be modified by interventions aimed at training-program design, reducing impact-related forces (eg, instructing an athlete to run "softer" or with a higher stride rate), and increasing the strength and/or endurance of local muscu …
The former is more amenable to intervention and may be modified by interventions aimed at training-program design, reducing impact-related f …
FGF23-related hypophosphatemic rickets/osteomalacia: diagnosis and new treatment.
Fukumoto S. Fukumoto S. J Mol Endocrinol. 2021 Feb;66(2):R57-R65. doi: 10.1530/JME-20-0089. J Mol Endocrinol. 2021. PMID: 33295878 Review.
Circulatory FGF23 is high in patients with these hypophosphatemic diseases while FGF23 is rather low in those with chronic hypophosphatemia from other causes such as vitamin D deficiency. These results indicate that FGF23 measurement is useful for the differential d …
Circulatory FGF23 is high in patients with these hypophosphatemic diseases while FGF23 is rather low in those with chronic hypophosphatemia …
Secondary Hyperparathyroidism: Pathogenesis and Latest Treatment.
Mizobuchi M, Ogata H, Koiwa F. Mizobuchi M, et al. Ther Apher Dial. 2019 Aug;23(4):309-318. doi: 10.1111/1744-9987.12772. Epub 2018 Dec 18. Ther Apher Dial. 2019. PMID: 30411503 Review.
In this process, many significant genetic findings have been established. Abnormalities of Ca-sensing receptor and vitamin D receptor are associated with the pathogenesis of SHPT, and fibroblast growth factor 23 has also been shown to be involved in the patho …
In this process, many significant genetic findings have been established. Abnormalities of Ca-sensing receptor and vitamin …
Expert panel consensus recommendations for diagnosis and treatment of secondary osteoporosis in children.
Galindo-Zavala R, Bou-Torrent R, Magallares-López B, Mir-Perelló C, Palmou-Fontana N, Sevilla-Pérez B, Medrano-San Ildefonso M, González-Fernández MI, Román-Pascual A, Alcañiz-Rodríguez P, Nieto-Gonzalez JC, López-Corbeto M, Graña-Gil J. Galindo-Zavala R, et al. Pediatr Rheumatol Online J. 2020 Feb 24;18(1):20. doi: 10.1186/s12969-020-0411-9. Pediatr Rheumatol Online J. 2020. PMID: 32093703 Free PMC article.
We believe it can serve as a useful tool that will contribute to the standardization of clinical practice for this pathology. Prophylactic measures, early diagnosis and a proper therapeutic approach are essential to improving bone health, not only in children and adolescen …
We believe it can serve as a useful tool that will contribute to the standardization of clinical practice for this pathology. Prophylactic m …
Executive summary of the 2017 KDIGO Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD) Guideline Update: what's changed and why it matters.
Ketteler M, Block GA, Evenepoel P, Fukagawa M, Herzog CA, McCann L, Moe SM, Shroff R, Tonelli MA, Toussaint ND, Vervloet MG, Leonard MB. Ketteler M, et al. Kidney Int. 2017 Jul;92(1):26-36. doi: 10.1016/j.kint.2017.04.006. Kidney Int. 2017. PMID: 28646995 Free article. Review.
This update, along with the 2009 publication, is intended to assist the practitioner caring for adults and children with chronic kidney disease (CKD), those on chronic dialysis therapy, or individuals with a kidney transplant. This review highlights key aspects of the 2017 …
This update, along with the 2009 publication, is intended to assist the practitioner caring for adults and children with chronic kidney dise …
Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management.
Charoenngam N, Nasr A, Shirvani A, Holick MF. Charoenngam N, et al. Genes (Basel). 2022 Oct 17;13(10):1880. doi: 10.3390/genes13101880. Genes (Basel). 2022. PMID: 36292765 Free PMC article. Review.
Hereditary metabolic bone diseases are characterized by genetic abnormalities in skeletal homeostasis and encompass one of the most diverse groups among rare diseases. ...Advances in molecular genetics and basic sciences has led to accurate genetic diagnosis and nov …
Hereditary metabolic bone diseases are characterized by genetic abnormalities in skeletal homeostasis and encompass one of the …
Natural Molecules in the Management of Polycystic Ovary Syndrome (PCOS): An Analytical Review.
Iervolino M, Lepore E, Forte G, Laganà AS, Buzzaccarini G, Unfer V. Iervolino M, et al. Nutrients. 2021 May 15;13(5):1677. doi: 10.3390/nu13051677. Nutrients. 2021. PMID: 34063339 Free PMC article. Review.
It is considered the most common endocrinological disorder, affecting up to 25% of women of reproductive age, and associated with long-term metabolic abnormalities predisposing to cardiovascular risk, such as insulin resistance (IR), dyslipidemia, endothelial dysfun …
It is considered the most common endocrinological disorder, affecting up to 25% of women of reproductive age, and associated with long-term …
Nutritional management in women with polycystic ovary syndrome: A review study.
Faghfoori Z, Fazelian S, Shadnoush M, Goodarzi R. Faghfoori Z, et al. Diabetes Metab Syndr. 2017 Nov;11 Suppl 1:S429-S432. doi: 10.1016/j.dsx.2017.03.030. Epub 2017 Apr 5. Diabetes Metab Syndr. 2017. PMID: 28416368 Review.
Polycystic ovary syndrome (PCOS) is endocrine disorder in women of reproductive age, which leads to reproductive, hormonal and metabolic abnormalities. Due to the presence of insulin resistance, PCOS increases the risk of chronic diseases like type 2 diabetes, hyper …
Polycystic ovary syndrome (PCOS) is endocrine disorder in women of reproductive age, which leads to reproductive, hormonal and metabolic …
137 results