Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1967 1
1972 1
1973 2
1974 2
1975 2
1976 1
1978 1
1979 5
1980 4
1981 3
1982 1
1985 3
1988 5
1989 8
1990 4
1991 5
1992 6
1993 4
1994 4
1995 5
1996 6
1997 10
1998 5
1999 6
2000 9
2001 5
2002 5
2003 4
2004 16
2005 11
2006 13
2007 14
2008 18
2009 25
2010 25
2011 13
2012 18
2013 17
2014 13
2015 13
2016 11
2017 13
2018 14
2019 20
2020 23
2021 29
2022 22
2023 16
2024 6

Text availability

Article attribute

Article type

Publication date

Search Results

414 results

Results by year

Filters applied: . Clear all
Page 1
Hungry bone syndrome.
Jain N, Reilly RF. Jain N, et al. Curr Opin Nephrol Hypertens. 2017 Jul;26(4):250-255. doi: 10.1097/MNH.0000000000000327. Curr Opin Nephrol Hypertens. 2017. PMID: 28375869 Review.
A severe drop in serum total calcium concentration less than 2.1 mmol/L and/or prolonged hypocalcemia for more than 4 days postparathyroidectomy is called hungry bone syndrome (HBS). Concomitant hypophosphatemia, hypomagnesemia, and hyperkalemia can be seen. Hypocalcemia a …
A severe drop in serum total calcium concentration less than 2.1 mmol/L and/or prolonged hypocalcemia for more than 4 days postparathyroidec …
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.
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is associated with severe complications such as rickets, lower limb deformities, pain, poor mineralization of the teeth and disproportionate short stature in children as well as hy …
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is associated with severe complications …
Recent and Emerging Therapies for Iron Deficiency in Anemia of CKD: A Review.
Bazeley JW, Wish JB. Bazeley JW, et al. Am J Kidney Dis. 2022 Jun;79(6):868-876. doi: 10.1053/j.ajkd.2021.09.017. Epub 2021 Nov 7. Am J Kidney Dis. 2022. PMID: 34758368 Review.
The proposed pathophysiology of 6H syndrome and hypophosphatemia is described. Ferric pyrophosphate citrate enables administration of iron for repletion through dialysate. Relative merits, costs, and risks of various iron agents such as hypersensitivity and 6H syndrome/ …
The proposed pathophysiology of 6H syndrome and hypophosphatemia is described. Ferric pyrophosphate citrate enables administration of …
Approach to treatment of hypophosphatemia.
Felsenfeld AJ, Levine BS. Felsenfeld AJ, et al. Am J Kidney Dis. 2012 Oct;60(4):655-61. doi: 10.1053/j.ajkd.2012.03.024. Epub 2012 Aug 3. Am J Kidney Dis. 2012. PMID: 22863286 Review.
Hypophosphatemia can be acute or chronic. Acute hypophosphatemia with phosphate depletion is common in the hospital setting and results in significant morbidity and mortality. Chronic hypophosphatemia, often associated with genetic or acquired renal ph
Hypophosphatemia can be acute or chronic. Acute hypophosphatemia with phosphate depletion is common in the hospital setting an
A clinician's guide to X-linked hypophosphatemia.
Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL. Carpenter TO, et al. J Bone Miner Res. 2011 Jul;26(7):1381-8. doi: 10.1002/jbmr.340. Epub 2011 May 2. J Bone Miner Res. 2011. PMID: 21538511 Free PMC article. Review.
X-linked hypophosphatemia (XLH) is the prototypic disorder of renal phosphate wasting, and the most common form of heritable rickets. ...
X-linked hypophosphatemia (XLH) is the prototypic disorder of renal phosphate wasting, and the most common form of heritable r …
X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management.
Baroncelli GI, Mora S. Baroncelli GI, et al. Front Endocrinol (Lausanne). 2021 Aug 6;12:688309. doi: 10.3389/fendo.2021.688309. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34421819 Free PMC article. Review.
It is caused by an impaired regulation of fibroblast growth factor 23 (FGF23) due to a PHEX gene mutation, which leads to reduced tubular reabsorption of phosphate and renal 1alpha-hydroxylase activity and increased renal 24-hydroxylase activity. Hypophosphatemia
It is caused by an impaired regulation of fibroblast growth factor 23 (FGF23) due to a PHEX gene mutation, which leads to reduced tubular re …
Tackling AKI: prevention, timing of dialysis and follow-up.
Vijayan A. Vijayan A. Nat Rev Nephrol. 2021 Feb;17(2):87-88. doi: 10.1038/s41581-020-00390-3. Nat Rev Nephrol. 2021. PMID: 33335277 Free PMC article. Review.
The STARRT-AKI trial demonstrated that early initiation of kidney replacement therapy for patients with AKI in intensive care units did not improve outcomes and was associated with a higher risk of hypotension and hypophosphatemia. Albuminuria at 90 days after a hospitaliz …
The STARRT-AKI trial demonstrated that early initiation of kidney replacement therapy for patients with AKI in intensive care units did not …
Rickets guidance: part I-diagnostic workup.
Haffner D, Leifheit-Nestler M, Grund A, Schnabel D. Haffner D, et al. Pediatr Nephrol. 2022 Sep;37(9):2013-2036. doi: 10.1007/s00467-021-05328-w. Epub 2021 Dec 15. Pediatr Nephrol. 2022. PMID: 34910242 Free PMC article. Review.
The latter are due to mutations in genes involved in vitamin D metabolism or action, renal phosphate reabsorption, or synthesis, or degradation of the phosphaturic hormone fibroblast growth factor 23 (FGF23). ...
The latter are due to mutations in genes involved in vitamin D metabolism or action, renal phosphate reabsorption, or synthesis, or d …
Calcium metabolism in health and disease.
Peacock M. Peacock M. Clin J Am Soc Nephrol. 2010 Jan;5 Suppl 1:S23-30. doi: 10.2215/CJN.05910809. Clin J Am Soc Nephrol. 2010. PMID: 20089499 Review.
Calcium balance refers to the state of the calcium body stores, primarily in bone, which are largely a function of dietary intake, intestinal absorption, renal excretion, and bone remodeling. Bone calcium balance can be positive, neutral, or negative, depending on a number …
Calcium balance refers to the state of the calcium body stores, primarily in bone, which are largely a function of dietary intake, intestina …
Newer formulations of intravenous iron: a review of their chemistry and key safety aspects - hypersensitivity, hypophosphatemia, and cardiovascular safety.
Blumenstein I, Shanbhag S, Langguth P, Kalra PA, Zoller H, Lim W. Blumenstein I, et al. Expert Opin Drug Saf. 2021 Jul;20(7):757-769. doi: 10.1080/14740338.2021.1912010. Epub 2021 May 15. Expert Opin Drug Saf. 2021. PMID: 33993818 Review.
Ferric derisomaltose (FDI; also known as iron isomaltoside), ferric carboxymaltose (FCM), and ferumoxytol (FER), are successful treatments for iron deficiency (Europe; FDI and FCM) and iron deficiency anemia (US; FDI, FCM, and FER).Areas covered: This review focusses on the chemi …
Ferric derisomaltose (FDI; also known as iron isomaltoside), ferric carboxymaltose (FCM), and ferumoxytol (FER), are successful treatments f …
414 results