Found: 14
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ETIOLOGY OF HYPERTENSION IN CHILDREN AND ADOLESCENTS.
- Published in:
- Lebanese Medical Journal, 2010, v. 58, n. 3, p. 142
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- Publication type:
- Article
Renal hypoprostaglandism, hypertension, and type IV renal tubular acidosis reversed by furosemide.
- Published in:
- 1983
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- Publication type:
- journal article
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 71, doi. 10.1038/79208
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- Publication type:
- Article
Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 4, p. 437, doi. 10.1515/jpem-2016-0338
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- Publication type:
- Article
Chronic Peritoneal Dialysis in Lebanese Children of Families with Low Socioeconomic Status.
- Published in:
- Peritoneal Dialysis International, 2015, v. 35, n. 1, p. 93, doi. 10.3747/pdi.2013.00342
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- Publication type:
- Article
Response to Steroids in Early-onset Nephrotic Syndrome.
- Published in:
- Saudi Journal of Kidney Diseases & Transplantation, 2013, v. 24, n. 3, p. 590, doi. 10.4103/1319-2442.111076
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- Publication type:
- Article
A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 4, p. 503, doi. 10.1007/s00467-006-0354-5
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- Publication type:
- Article
Pamidronate Rescue Therapy for Hypercalcemia in a Child with Williams Syndrome.
- Published in:
- Frontiers in Endocrinology, 2018, p. 1, doi. 10.3389/fendo.2018.00240
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- Publication type:
- Article
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
- Published in:
- Nature, 2012, v. 482, n. 7383, p. 98, doi. 10.1038/nature10814
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- Publication type:
- Article
Ureteropelvic Junction Obstruction and Parathyroid Adenoma: A Case Report and Literature Review.
- Published in:
- 2017
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- Publication type:
- Case Study
Editorial: Hereditary and acquired disorders of calcium homeostasis.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.1124762
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- Publication type:
- Article
Norovirus: a novel etiologic agent in hemolytic uremic syndrome in an infant.
- Published in:
- 2019
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- Publication type:
- journal article
Mutations in the gene encoding B1 subunit of H<sup>+</sup>-ATPase cause renal tubular acidosis with sensorineural deafness.
- Published in:
- Nature Genetics, 1999, v. 21, n. 1, p. 84, doi. 10.1038/5022
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- Publication type:
- Article
Distinctive vasculopathy with systemic involvement due to levamisole long-term therapy: a case report.
- Published in:
- 2018
- By:
- Publication type:
- journal article