LE WE PMID CA
Kidney (Malformation)7569Niere (Fehlbildung)

Acidosis (renal tubular)

ACTN4 Alpha actinin4

ADH AVP Vasopressin

Autonomous nervous system (Afferents visceral)

Bartter s syndrome

CASR

CD2AP

CFHR5

CLC Kb

ClC5

Cystinosis

Cystinuria

Dent s syndrome

Goldenhar s syndrome

Hypercalciuric nephrolithiasis with hypophosphatemia

Hypocalciemic hypercalciuria autosomal dominant

Hypomagnesemia with hypercalciuria familiar

Kidney (Glomerulus)

Kidney (Malformation)

Kidney (Minimal change nephrotic syndrome)

Kidney (Podocytes)

Kidney (Principal cells)

Kidney (Registry of Diseases)

Mitochondria (Mitochondriopathy)

Neph1

Nephrocalcinosis

Nephrolithiasis

NPHS1 Nephrin

NPT2c

Osmosensor

Paracellin1

Phosphate (Hypophosphatemia)

Podocin

Prenatal diagnostics

Toxicology (BASKET)

TRPC6

TRPM6

TRPV1

TRPV4

Water (Physiology renal)

2004  
1
The developing kidney and environmental toxins.
[15060203] Pediatrics 113(4 Suppl): 1084-91 (2004)
2010  
2
Renal malformations associated with mutations of developmental genes: messages from the clinic.
[20603712] Pediatr Nephrol 25(11): 2247-55 (2010)
2010  
3
Molecular anatomy of the kidney: what have we learned from gene expression and functional genomics?
[20049614] Pediatr Nephrol 25(6): 1005-16 (2010)
2007  
4
Genetic approaches to human renal agenesis/hypoplasia and dysplasia.
[17437132] Pediatr Nephrol 22(10): 1675-84 (2007)
2009  
5
Postnatal evaluation of infants with an abnormal antenatal renal sonogram.
[19663038] Curr Opin Pediatr 21(2): 207-13 (2009)
2007  
6
2010  
7
2003  
8
Podocyte differentiation and hereditary proteinuria/nephrotic syndromes.
[12761234] J Am Soc Nephrol 14 Suppl 1(-): S22-6 (2003)
2010  
9
Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.
[20333530] Pediatr Nephrol 25(9): 1621-32 (2010)
2009  
10
Genetic causes of hypercalciuric nephrolithiasis.
[18446382] Pediatr Nephrol 24(12): 2321-32 (2009)
1993  
11
A molecular approach to inherited kidney disorders.
[8301921] Kidney Int 44(6): 1205-16 (1993)
1988  
12
Overview of pediatric nephropathology.
[3292815] Kidney Int 33(5): 1016-32 (1988)
1966  
13
Paediatric nephrology: scientific study of kidneys and their diseases in infants and children.
[5328623] Arch Dis Child 41(217): 229-37 (1966)
2004  
14
Evolving concepts in human renal dysplasia.
[15034102] J Am Soc Nephrol 15(4): 998-1007 (2004)
1975  
15
Renal dysplasia in nephrectomy specimens from adolescents and adults.
[1236628] J Clin Pathol 28(11): 879-90 (1975)
2003  
16
Advances in genetic detection of kidney disease.
[17657098] Saudi J Kidney Dis Transpl 14(3): 259-75 (2003)
2003  
17
2003  
18
Cystinosis and cystinuria: differences in outcome.
[17657107] Saudi J Kidney Dis Transpl 14(3): 351-7 (2003)
2003  
19
Hereditary Hypokalemic Salt-losing Tubular Disorders.
[17657111] Saudi J Kidney Dis Transpl 14(3): 386-97 (2003)
2008  
20
Renal function and mitochondrial cytopathy (MC): more questions than answers?
[18487272] QJM 101(10): 755-66 (2008)
2011  
21
Relapsing typhilitis to CFHR5 nephropathy: the thrill of discovery.
[21558093] J R Soc Med 104(5): 181 (2011)
2007  
22
Genetics of hypercalciuric stone forming diseases.
[17687260] Kidney Int 72(9): 1065-72 (2007)
2012  
23
Physiopathology of hereditary polyuric states: a molecular view of renal function.
[22802123] Swiss Med Wkly 142(): w13613 (2012)
2002  
24
Clinical and genetic epidemiology of inherited renal disease in Newfoundland.
[12028433] Kidney Int 61(6): 1925-34 (2002)
2010  
25
2009  
26
New concepts in pathogenesis of renal hypophosphatemic syndromes.
[19377250] Iran J Kidney Dis 3(1): 1-6 (2009)
2010  
27
Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes.
[20969579] Ann N Y Acad Sci 1214(): 83-98 (2010)
2010  
28
Goldenhar syndrome: clinical features with orofacial emphasis.
[21308299] J Appl Oral Sci 18(6): 646-9 (2010)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.



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