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» Authors » C E Kashtan

C E Kashtan

Explore the profile of C E Kashtan including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 75
Citations 1732
Followers 0
Related Specialties
Nephrology
Pediatrics
General Surgery
Top 10 Co-Authors
A F Michael
Y Kim
A J Matas
S M MAUER
T E Nevins
M M Kleppel
B M Chavers
K J Gillingham
Y Sado
K Tryggvason
Published In
Pediatr Nephrol
Kidney Int
J Am Soc Nephrol
Kidney Int Suppl
Transplantation
Affiliations
Soon will be listed here.
Recent Articles
1.
Characterization of the genetic basis for autosomal recessive hereditary nephropathy in the English Springer Spaniel
Nowend K, Starr-Moss A, Lees G, Berridge B, Clubb F, Kashtan C, et al.
J Vet Intern Med . 2012 Feb; 26(2):294-301. PMID: 22369189
Background: Autosomal recessive hereditary nephropathy (ARHN) was diagnosed in 2 English Springer Spaniels (ESS), a breed not previously reported to be affected by hereditary nephropathy (HN). Objective: To identify and...
2.
Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)
Meloni I, Vitelli F, Pucci L, Lowry R, Tonlorenzi R, Rossi E, et al.
J Med Genet . 2002 May; 39(5):359-65. PMID: 12011158
No abstract available.
3.
Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes
Kashtan C
Contrib Nephrol . 2001 Nov; (136):79-99. PMID: 11688406
No abstract available.
4.
Alport syndrome: renal transplantation and donor selection
Kashtan C
Ren Fail . 2000 Dec; 22(6):765-8. PMID: 11104164
No abstract available.
5.
Alport syndrome: abnormalities of type IV collagen genes and proteins
Kashtan C
Ren Fail . 2000 Dec; 22(6):737-49. PMID: 11104161
No abstract available.
6.
Alport syndromes: phenotypic heterogeneity of progressive hereditary nephritis
Kashtan C
Pediatr Nephrol . 2000 Jun; 14(6):502-12. PMID: 10872195
Alport syndrome is a primary genetic disease of basement membranes, manifested clinically as a progressive nephropathy variably associated with sensorineural deafness and a plethora of ocular abnormalities. The long-recognized phenotypic...
7.
Expression of the alpha6 chain of type IV collagen in glomerular basement membranes of healthy adult dogs
Lees G, Kashtan C, Michael A, Helman R, Naito I, Ninomiya Y, et al.
Am J Vet Res . 2000 Jan; 61(1):38-41. PMID: 10630775
Objective: To evaluate expression of the alpha6 chain of type IV collagen in the glomerular basement membranes (GBM) of healthy dogs. Sample Population: Kidney specimens from 12 healthy dogs. For...
8.
Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndrome
Schimmenti L, Shim H, Wirtschafter J, Panzarino V, Kashtan C, Kirkpatrick S, et al.
Hum Mutat . 1999 Oct; 14(5):369-76. PMID: 10533062
Renal-Coloboma syndrome, an autosomal dominant disorder characterized by colobomatous eye defects, vesicoureteral reflux, and abnormal kidneys, results from mutations in PAX2. The purpose of this study was to identify mutations...
9.
Recurrent bacteremia with enteric pathogens in recessive polycystic kidney disease
Kashtan C, Primack W, Kainer G, Rosenberg A, McDonald R, Warady B
Pediatr Nephrol . 1999 Sep; 13(8):678-82. PMID: 10502126
Eight children with autosomal recessive polycystic kidney disease (ARPKD) and recurrent bacteremia with enteric pathogens are described. Typical clinical features of bacterial cholangitis were absent, although in five patients histological...
10.
Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes
Kashtan C
Medicine (Baltimore) . 1999 Sep; 78(5):338-60. PMID: 10499074
Alport syndrome (AS) is a genetically heterogeneous disease arising from mutations in genes coding for basement membrane type IV collagen. About 80% of AS is X-linked, due to mutations in...