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2005, ISBN 9780192632432, xii, 221
Lesions of the oral cavity have an enormous impact on the quality of life of patients with advanced disease. They cause considerable morbidity and diminish a... 
Palliative Care | Mouth Diseases | Chronic Disease | therapy | methods | palliative medicine | Advanced disease | Oral cavity | Anorexia | Oral complications | Oral nutrition | Lesions | Malnutrition | Patients | Morbidity | Quality of life
Book
Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, ISSN 1079-2104, 1995
Journal
2009, 3rd ed., ISBN 1416034358, xvi, 968
Book
Pediatric Clinics of North America, ISSN 0031-3955, 02/2019, Volume 66, Issue 1, pp. 169 - 178
Dent disease is an X-linked form of chronic kidney disease characterized by hypercalciuria, low molecular weight proteinuria, nephrocalcinosis, and proximal... 
CLCN5 | Chronic kidney disease | Dent disease | Nephrolithiasis | OCRL1 | CHILDREN | OCRL1 MUTATIONS | HYPERCALCIURIA | CHLORIDE CHANNEL GENE | MOUSE MODEL | MOLECULAR-WEIGHT PROTEINURIA | NEPHROCALCINOSIS | PEDIATRICS | KIDNEY | Dent Disease - physiopathology | Dent Disease - diagnosis | Diagnosis, Differential | Dent Disease - genetics | Humans | Dent Disease - therapy | Child | Disease Progression
Journal Article
2013, 1. Aufl., ISBN 9781405153652, x, 446
"This pioneering book is uniquely dedicated to oral hard tissue pathology. It presents the growth of clinical knowledge and advancement in the field, along... 
pathology | Tooth Diseases | Abnormalities | therapy | Teeth | prevention & control | Diseases | Other branches of medicine | Oral Pathology | Dental therapeutics
Book
2003, 4th ed., ISBN 0192632795, xiii, 272
Book
Pediatric Nephrology, ISSN 0931-041X, 10/2013, Volume 28, Issue 10, pp. 1923 - 1942
Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and... 
Pediatrics | Nephrocalcinosis | Dent disease | Hereditary disorders | Crystalline nephropathy | Nephrolithiasis | Cystinuria | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis | Kidney failure | Medicine & Public Health | Adenine phosphoribosyltransferase deficiency | Primary hyperoxaluria | 2,8-dihydroxyadeninuria | GENOTYPE-PHENOTYPE CORRELATION | I PRIMARY HYPEROXALURIA | HUMAN APRT GENE | KNOCKOUT MOUSE MODEL | FAMILIAL HYPOMAGNESEMIA | PRIMARY HYPEROXALURIA TYPE-1 | URINARY OXALATE EXCRETION | RENAL CHLORIDE CHANNEL | UROLOGY & NEPHROLOGY | PEDIATRICS | DENTS-DISEASE | Hypercalciuria - epidemiology | Humans | Dent Disease - therapy | Renal Insufficiency, Chronic - epidemiology | Renal Insufficiency, Chronic - therapy | Dent Disease - genetics | Renal Insufficiency, Chronic - genetics | Renal Insufficiency, Chronic - diagnosis | Dent Disease - epidemiology | Child | Cystinuria - diagnosis | Genetic Predisposition to Disease | Adenine Phosphoribosyltransferase - genetics | Risk Factors | Heredity | Nephrocalcinosis - therapy | Hyperoxaluria, Primary - epidemiology | Hyperoxaluria, Primary - genetics | Metabolism, Inborn Errors - diagnosis | Phenotype | Kidney Calculi - therapy | Nephrocalcinosis - genetics | Cystinuria - epidemiology | Nephrocalcinosis - diagnosis | Kidney Calculi - genetics | Urolithiasis - genetics | Cystinuria - therapy | Prognosis | Hyperoxaluria, Primary - diagnosis | Nephrocalcinosis - epidemiology | Metabolism, Inborn Errors - epidemiology | Metabolism, Inborn Errors - therapy | Renal Tubular Transport, Inborn Errors - genetics | Hyperoxaluria, Primary - therapy | Dent Disease - diagnosis | Renal Tubular Transport, Inborn Errors - epidemiology | Adenine Phosphoribosyltransferase - deficiency | Hypercalciuria - genetics | Renal Tubular Transport, Inborn Errors - diagnosis | Hypercalciuria - therapy | Hypercalciuria - diagnosis | Renal Tubular Transport, Inborn Errors - therapy | Metabolism, Inborn Errors - genetics | Cystinuria - genetics | Urolithiasis - therapy | Kidney Calculi - diagnosis | Animals | Urolithiasis - epidemiology | Kidney Calculi - epidemiology | Urolithiasis - diagnosis | Causes of | Genetic aspects | Research | Chronic kidney failure | Kidney stones | nephrocalcinosis | kidney failure | hereditary disorders | adenine phosphoribosyltransferase deficiency | cystinuria | primary hyperoxaluria | crystalline nephropathy | familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Journal Article
Kidney International, ISSN 0085-2538, 08/2016, Volume 90, Issue 2, pp. 430 - 439
Journal Article
2016, Eleventh edition, ISBN 0323096352, xiv, 907
Find the latest evidence-based research and clinical treatments!Cohen's Pathways of the Pulp, 11th Edition covers the science, theory, and practice of... 
Endodontics | Dental pulp | Diseases
Book
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