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Nature, ISSN 0028-0836, 02/2012, Volume 482, Issue 7383, pp. 98 - 102
Journal Article
Journal Medical Libanais, ISSN 0023-9852, 07/2010, Volume 58, Issue 3, pp. 142 - 145
While most hypertension in children has been previously considered secondary to renal, cardiovascular or endocrine etiology, a substantial number of children... 
Child | Humans | Adolescent | Hypertension - etiology
Journal Article
Frontiers in Endocrinology, ISSN 1664-2392, 05/2018, Volume 9, Issue MAY, p. 240
A 15-month-old male infant diagnosed with Williams Syndrome (WS) was admitted with severe hypercalcemia and nephrocalcinosis. Intravenous hydration and... 
Hypercalcemia | Pamidronate | Nephrocalcinosis | Furosemide | Williams syndrome | hypercalcemia | pamidronate | BEUREN-SYNDROME | BISPHOSPHONATES | LONG-TERM CONTROL | nephrocalcinosis | ENDOCRINOLOGY & METABOLISM | furosemide | INFUSION | Usage | Care and treatment | Research | Disodium pamidronate | Risk factors
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2000, Volume 26, Issue 1, pp. 71 - 75
The multi-subunit H+-ATPase pump is present at particularly high density on the apical (luminal) surface of α-intercalated cells of the cortical collecting... 
H+-ATPASE | GENE | HYPERTENSION | LINKAGE | VPH1P | GENETICS & HEREDITY | Protein Biosynthesis | Kidney - pathology | Humans | Acidosis, Renal Tubular - genetics | Child, Preschool | Male | Proton Pumps - biosynthesis | Brain - metabolism | Polymorphism, Single-Stranded Conformational | Tissue Distribution | Kidney - metabolism | Recombination, Genetic | Gene Deletion | Suppressor Factors, Immunologic | Child | Amino Acid Sequence | Physical Chromosome Mapping | Proton Pumps - chemistry | Adenosine Triphosphatases - metabolism | Acidosis, Renal Tubular - urine | Genetic Markers | Chromosomes, Human, Pair 7 | Polymorphism, Genetic | Mitochondrial Proton-Translocating ATPases | Proton-Translocating ATPases | Protein Isoforms | Adolescent | Adenosine Triphosphatases - genetics | Contig Mapping | Hearing - physiology | Models, Genetic | Mutation | Proton Pumps - genetics | Audiometry | Exons | Kidney Cortex - metabolism | Molecular Sequence Data | Pregnancy Proteins | RNA Splicing | Adult | Female | Vacuolar Proton-Translocating ATPases | Genetic Linkage | Hearing - genetics | Genes, Recessive | Acidosis, Renal Tubular - metabolism | Sequence Homology, Amino Acid | Homozygote | Blotting, Northern | Pedigree | DNA, Complementary - metabolism | Microscopy, Fluorescence | Complications and side effects | Gene mutations | Physiological aspects | Research | Diagnosis | Acidosis | Risk factors | Membrane proteins | ATP6N1B gene
Journal Article
Medical Humanities, ISSN 0017-5749, 07/1995, Volume 37, Issue 1, p. 63
It has been suggested that antibodies to a colonocyte protein of 40 kD (an intestinal isoform of tropomyosin) are specifically found in the serum and mucosa of... 
Journal Article
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, ISSN 1319-2442, 07/2003, Volume 14, Issue 3, p. 305
Journal Article
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 1999, Volume 19, Issue 1, pp. 4 - 7
Background: Primary hyperoxaluria type I (PHI) is a rare metabolic disease caused by deficiency or abnormalities of the peroxisomal enzyme alanine-glyoxylate... 
End-stage renal disease | Nephrocalcinosis | Nephrolithiasis | Primary hyperoxaluria type I (PHI) | primary hyperoxaluria type I (PHI) | MEDICINE, GENERAL & INTERNAL | PYRIDOXINE | LIVER-TRANSPLANTATION | MANAGEMENT | KIDNEY-TRANSPLANTATION | nephrocalcinosis | PRIMARY OXALOSIS | nephrolithiasis | end-stage renal disease | REGISTRY
Journal Article
Book Chapter
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