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1981 1
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Page 1
Intellectual Disability and Psychotropic Medications.
Herzig L, de Lacy N, Capone G, Radesky J. Herzig L, et al. J Dev Behav Pediatr. 2018 Sep;39(7):591-593. doi: 10.1097/DBP.0000000000000613. J Dev Behav Pediatr. 2018. PMID: 30134288
Currently, he struggles with constipation, esophageal strictures, medullary nephrocalcinosis, urinary retention, sleep dysregulation, G-tube dependency, and hip dysplasia.Andrew walked at 11 to 12 years of age. ...
Currently, he struggles with constipation, esophageal strictures, medullary nephrocalcinosis, urinary retention, sleep dysregu …
Medullary nephrocalcinosis in nephropathic cystinosis.
Theodoropoulos DS, Shawker TH, Heinrichs C, Gahl WA. Theodoropoulos DS, et al. Pediatr Nephrol. 1995 Aug;9(4):412-8. doi: 10.1007/BF00866713. Pediatr Nephrol. 1995. PMID: 7577398 Clinical Trial.
We also retrospectively analyzed parameters of calcium and phosphate metabolism representing 216 person-years of data on these children. Fifteen children had no evidence of medullary nephrocalcinosis, while 18 had mild nephrocalcinosis, and 8 severe nephrocalcinosis …
We also retrospectively analyzed parameters of calcium and phosphate metabolism representing 216 person-years of data on these children. Fif …
Medullary nephrocalcinosis in Schimke immuno-osseous dysplasia.
Yavuz S, Bayazıt AK, Anarat A, Gonlusen G, Alsancak P. Yavuz S, et al. Pediatr Int. 2015 Apr;57(2):310-3. doi: 10.1111/ped.12455. Pediatr Int. 2015. PMID: 25868949
The most common renal pathology is focal segmental glomerulosclerosis (FSGS). Medullary nephrocalcinosis refers to the diffuse deposition of calcium salts in renal medulla and has not previously been identified in SIOD. Here we report the first case of a pediatric p …
The most common renal pathology is focal segmental glomerulosclerosis (FSGS). Medullary nephrocalcinosis refers to the diffuse …
Medullary nephrocalcinosis associated with long-term furosemide abuse in adults.
Kim YG, Kim B, Kim MK, Chung SJ, Han HJ, Ryu JA, Lee YH, Lee KB, Lee JY, Huh W, Oh HY. Kim YG, et al. Nephrol Dial Transplant. 2001 Dec;16(12):2303-9. doi: 10.1093/ndt/16.12.2303. Nephrol Dial Transplant. 2001. PMID: 11733620
Kidney biopsies performed in three patients showed focal tubulo-interstitial fibrosis and atrophy and calcifications were observed in outer medullary tubulo-interstitium. CONCLUSIONS: Long-term furosemide abuse can cause medullary nephrocalcinosis in adults, and the …
Kidney biopsies performed in three patients showed focal tubulo-interstitial fibrosis and atrophy and calcifications were observed in outer …
Metabolic and histologic investigation of the nature of nephrocalcinosis in children with hypophosphatemic rickets and in the Hyp mouse.
Alon U, Donaldson DL, Hellerstein S, Warady BA, Harris DJ. Alon U, et al. J Pediatr. 1992 Jun;120(6):899-905. doi: 10.1016/s0022-3476(05)81957-2. J Pediatr. 1992. PMID: 1317418
Mice in the experimental group excreted more phosphate (p less than 0.001) and less calcium (p less than 0.01) than control mice did, and medullary nephrocalcinosis, with a high kidney calcium content, developed (p less than 0.001). ...
Mice in the experimental group excreted more phosphate (p less than 0.001) and less calcium (p less than 0.01) than control mice did, and …
Nephrocalcinosis and its relationship to treatment of hereditary rickets.
Goodyer PR, Kronick JB, Jequier S, Reade TM, Scriver CR. Goodyer PR, et al. J Pediatr. 1987 Nov;111(5):700-4. doi: 10.1016/s0022-3476(87)80245-7. J Pediatr. 1987. PMID: 2822887
A pattern of increased echogenicity of the renal pyramids (ERP) was identified in 11/23 patients with XLH and 3/11 patients with ARVDD; this ultrasonographic finding has previously been associated with medullary nephrocalcinosis. Patients with XLH and ERP had signif …
A pattern of increased echogenicity of the renal pyramids (ERP) was identified in 11/23 patients with XLH and 3/11 patients with ARVDD; this …
High incidence of nephrocalcinosis in extremely preterm infants treated with dexamethasone.
Cranefield DJ, Odd DE, Harding JE, Teele RL. Cranefield DJ, et al. Pediatr Radiol. 2004 Feb;34(2):138-42. doi: 10.1007/s00247-003-1090-7. Epub 2003 Nov 18. Pediatr Radiol. 2004. PMID: 14624322 Clinical Trial.
BACKGROUND: The use of postnatal corticosteroids to treat or prevent chronic lung disease is common in very preterm infants. Medullary nephrocalcinosis has been noted as a possible side effect. ...PATIENTS AND METHODS: A prospective study of extremely preterm infant …
BACKGROUND: The use of postnatal corticosteroids to treat or prevent chronic lung disease is common in very preterm infants. Medullary …
Medullary nephrocalcinosis and pancreatic calcifications demonstrated by ultrasound and CT in infants after treatment with ACTH.
Rausch HP, Hanefeld F, Kaufmann HJ. Rausch HP, et al. Radiology. 1984 Oct;153(1):105-7. doi: 10.1148/radiology.153.1.6089261. Radiology. 1984. PMID: 6089261
Nine patients were found to have appearances characteristic of medullary nephrocalcinosis. In each of these infants the cortical echogenicity was normal in the presence of focal areas of increased echogenicity within the renal pyramids. ...
Nine patients were found to have appearances characteristic of medullary nephrocalcinosis. In each of these infants the cortic …
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
Alparslan C, Öncel EP, Akbay S, Alaygut D, Mutlubaş F, Tatlı M, Konrad M, Yavaşcan Ö, Kasap-Demir B. Alparslan C, et al. Turk J Pediatr. 2018;60(1):76-80. doi: 10.24953/turkjped.2018.01.011. Turk J Pediatr. 2018. PMID: 30102483 Free article.
Laboratory findings revealed hypocalcemia and hypomagnesemia. Bilateral medullary nephrocalcinosis was detected on abdominal ultrasound. His ophthalmologic examination was unremarkable. ...Biochemistry profile revealed hypocalcemia and hypomagnesemia. Urinary calciu …
Laboratory findings revealed hypocalcemia and hypomagnesemia. Bilateral medullary nephrocalcinosis was detected on abdominal u …
Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies.
Reinalter SC, Gröne HJ, Konrad M, Seyberth HW, Klaus G. Reinalter SC, et al. J Pediatr. 2001 Sep;139(3):398-406. doi: 10.1067/mpd.2001.117007. J Pediatr. 2001. PMID: 11562620 Clinical Trial.
The median creatinine clearance rose from 67.4 to 96.5 mL/min/1.73 m(2) (P <.05) but remained subnormal in 4 patients. Ultrasonography elucidated medullary nephrocalcinosis in 8 patients. Renal tissue showed slight/moderate focal tubular atrophy and interstitial …
The median creatinine clearance rose from 67.4 to 96.5 mL/min/1.73 m(2) (P <.05) but remained subnormal in 4 patients. Ultrasonography el …
23 results