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Quoted phrase not found in phrase index: "Abnormal renal tubular resorption"
Page 1
Non-crystalline light chain proximal tubulopathy, a morphologically protean entity.
Kousios A, Blakey S, Moran L, Atta M, Charif R, Duncan N, Smith A, Tam FWK, Levy JB, Chaidos A, Roufosse C. Kousios A, et al. Nephrol Dial Transplant. 2023 Oct 31;38(11):2576-2588. doi: 10.1093/ndt/gfad085. Nephrol Dial Transplant. 2023. PMID: 37120733 Free PMC article.
Only six patients had known haematological disease at the time of renal biopsy. Multiple myeloma (MM) was diagnosed in seven patients cases and monoclonal gammopathy of renal significance (MGRS) in five patients. ...Patients who achieved haematological response (inc …
Only six patients had known haematological disease at the time of renal biopsy. Multiple myeloma (MM) was diagnosed in seven patients …
The idiopathic hypercalciuria reviewed. Metabolic abnormality or disease?
García Nieto VM, Luis Yanes MI, Tejera Carreño P, Perez Suarez G, Moraleda Mesa T. García Nieto VM, et al. Nefrologia (Engl Ed). 2019 Nov-Dec;39(6):592-602. doi: 10.1016/j.nefro.2019.02.011. Epub 2019 May 31. Nefrologia (Engl Ed). 2019. PMID: 31160051 Free article. Review. English, Spanish.
The discovery of genetic hypercalciuric stone-forming rats has allowed us to glimpse the pathophysiological mechanism of IH since they show many data in common with humans with IH as normal levels of blood calcium, intestinal calcium hyperabsorption, increased bone resorption
The discovery of genetic hypercalciuric stone-forming rats has allowed us to glimpse the pathophysiological mechanism of IH since they show …
Spectrum of renal dysfunction after curative parathyroidectomy in symptomatic primary hyperparathyroidism.
Gosavi V, Lila A, Memon SS, Sarathi V, Goroshi M, Jamale T, Thakare S, Phadte A, Patil V, Bandgar T. Gosavi V, et al. Ann Endocrinol (Paris). 2023 Feb;84(1):14-20. doi: 10.1016/j.ando.2022.10.015. Epub 2022 Dec 20. Ann Endocrinol (Paris). 2023. PMID: 36563936
We aimed to assess renal glomerular and tubular functions in an sPHPT cohort at 1 year's follow-up. ...Further studies are warranted to understand the clinical implications of these various renal abnormalities....
We aimed to assess renal glomerular and tubular functions in an sPHPT cohort at 1 year's follow-up. ...Further studies are war …
Autosomal dominant polycystic kidney disease (ADPKD)--mechanisms of cyst formation and renal failure.
Ritz E, Zeier M, Geberth S, Waldherr R. Ritz E, et al. Aust N Z J Med. 1993 Feb;23(1):35-41. doi: 10.1111/j.1445-5994.1993.tb00535.x. Aust N Z J Med. 1993. PMID: 8460972 Review.
None of the hypotheses proposed so far to explain cyst formation in autosomal dominant polycystic kidney disease (ADPKD) is entirely satisfactory, e.g. the theory of tubular obstruction by intraluminal polyps or dilatation of nephron segments as a consequence of abnorma
None of the hypotheses proposed so far to explain cyst formation in autosomal dominant polycystic kidney disease (ADPKD) is entirely satisfa …
Osteomalacic and hyperparathyroid changes in fibrous dysplasia of bone: core biopsy studies and clinical correlations.
Corsi A, Collins MT, Riminucci M, Howell PG, Boyde A, Robey PG, Bianco P. Corsi A, et al. J Bone Miner Res. 2003 Jul;18(7):1235-46. doi: 10.1359/jbmr.2003.18.7.1235. J Bone Miner Res. 2003. PMID: 12854833 Free article.
INTRODUCTION: Fibrous dysplasia is a genetic noninherited disease caused by activating mutations of the GNAS1 gene, resulting in the deposition of qualitatively abnormal bone and marrow. This study was designed to learn more about the local processes of bone deposition, mi …
INTRODUCTION: Fibrous dysplasia is a genetic noninherited disease caused by activating mutations of the GNAS1 gene, resulting in the deposit …
The utility of (99m)Tc-DMSA and Tc(99m)-EC scintigraphy for early diagnosis of ifosfamide induced nephrotoxicity.
Caglar M, Yarís N, Akyuz C. Caglar M, et al. Nucl Med Commun. 2001 Dec;22(12):1325-32. doi: 10.1097/00006231-200112000-00008. Nucl Med Commun. 2001. PMID: 11711903
In this study, we investigated the toxic effects of ifosfamide and cisplatin by clinical and biochemical parameters in relation to (99m)Tc-dimercaptosuccinic acid ((99m)Tc-DMSA) and Tc(99m)N, N-ethylenedicysteine (EC) renal scintigraphy. The indicators were urinary beta2-m …
In this study, we investigated the toxic effects of ifosfamide and cisplatin by clinical and biochemical parameters in relation to (99m)Tc-d …
Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report.
Shamsian BS, Momtazmanesh N, Saneifard H, Tabatabaei SMTH, Jafari M, Pour ZK, Al-Hussieni KJMR, Jamee M, Kamfar S. Shamsian BS, et al. Pediatr Transplant. 2024 May;28(3):e14689. doi: 10.1111/petr.14689. Pediatr Transplant. 2024. PMID: 38655726
Later at 9 months old, he was found to have eye disorder such as nystagmus, fracture of the elbow, abnormal skeletal survey, normal cell blood count (CBC), and severe hypocellularity in the bone marrow. Further evaluation showed renal tubular acidosis type 2. …
Later at 9 months old, he was found to have eye disorder such as nystagmus, fracture of the elbow, abnormal skeletal survey, normal c …
Alteration of noncollagenous bone matrix proteins in distal renal tubular acidosis.
Disthabanchong S, Domrongkitchaiporn S, Sirikulchayanonta V, Stitchantrakul W, Karnsombut P, Rajatanavin R. Disthabanchong S, et al. Bone. 2004 Sep;35(3):604-13. doi: 10.1016/j.bone.2004.04.028. Bone. 2004. PMID: 15336595
Our previous report on bone histomorphometry in patients with distal renal tubular acidosis (dRTA) revealed decreased bone formation rate (BFR) when compared to healthy subjects. ...Six of seven patients had decreased osteopontin expression. In conclusion, the ab
Our previous report on bone histomorphometry in patients with distal renal tubular acidosis (dRTA) revealed decreased bone for …
Amelioration of hypophosphatemic rickets and osteoporosis with pamidronate and growth hormone in Lowe syndrome.
Hou JW. Hou JW. J Formos Med Assoc. 2009 Sep;108(9):730-5. doi: 10.1016/S0929-6646(09)60397-1. J Formos Med Assoc. 2009. PMID: 19773212 Free article.
The oculocerebrorenal syndrome of Lowe, an X-linked multisystem disorder, was diagnosed in a male patient who presented with typical abnormalities of the eyes, kidneys and nervous system. Besides congenital cataracts, renal tubular dysfunction and psyc …
The oculocerebrorenal syndrome of Lowe, an X-linked multisystem disorder, was diagnosed in a male patient who presented with typical abno
Technetium-99m dimercaptosuccinic acid and ifosfamide tubular dysfunction in children with cancer.
Anninga JK, Valdés Olmos RA, de Kraker J, van Tinteren H, Hoefnagel CA, van Royen EA. Anninga JK, et al. Eur J Nucl Med. 1994 Jul;21(7):658-62. doi: 10.1007/BF00285589. Eur J Nucl Med. 1994. PMID: 7957353
Quantitative 99mTc-dimercaptosuccinic acid (99mTc-DMSA) renal scintigraphy was used to asses ifosfamide-induced changes in renal function in 11 children who received chemotherapy for various malignancies. ...A highly significant relationship between 99mTc-DMSA uptak …
Quantitative 99mTc-dimercaptosuccinic acid (99mTc-DMSA) renal scintigraphy was used to asses ifosfamide-induced changes in renal
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