Renal AND Polycystic kidney diseasehttp://www.unboundmedicine.com/medline/ebm/research/Renal/Polycystic_kidney_diseaseUnbound MEDLINE is a service provided by Unbound Medicine, Inc. that includes data and services from the U.S. National Library of Medicine's MEDLINE® and PubMed® databases.en-usUnbound Medicine, Inc.Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region.http://www.unboundmedicine.com/medline/ebm/record/19050042/full_citation/Localization_of_Inv_in_a_distinctive_intraciliary_compartment_requires_the_C_terminal_ninein_homolog_containing_region_Shiba D, Yamaoka Y, Hagiwara H, et al. 
Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region. [JOURNAL ARTICLE]
J Cell Sci 2008 Dec 2.
Abstract | Full CitationComparison between ultrasound and genetic testing for the early diagnosis of polycystic kidney disease in Persian and Exotic Shorthair cats.http://www.unboundmedicine.com/medline/ebm/record/19046910/full_citation/Comparison_between_ultrasound_and_genetic_testing_for_the_early_diagnosis_of_polycystic_kidney_disease_in_Persian_and_Exotic_Shorthair_cats_Bonazzi M, Volta A, Gnudi G, et al. 
Comparison between ultrasound and genetic testing for the early diagnosis of polycystic kidney disease in Persian and Exotic Shorthair cats. [JOURNAL ARTICLE]
J Feline Med Surg 2008 Nov 27.
Abstract | Full Citation | Find Related Articles Chloroform deposition in renal cyst fluid of hemodialysis patients with renal cystic disorders.http://www.unboundmedicine.com/medline/ebm/record/19042963/full_citation/Chloroform_deposition_in_renal_cyst_fluid_of_hemodialysis_patients_with_renal_cystic_disorders_Ito F, Nakazawa H, Ohsaka Y, et al. 
Chloroform deposition in renal cyst fluid of hemodialysis patients with renal cystic disorders. [Journal Article]
Hum Exp Toxicol 2008 Oct; 27(10):769-72.
Abstract | Full CitationRhombencephalosynapsis associated with autosomal dominant polycystic kidney disease Type 1.http://www.unboundmedicine.com/medline/ebm/record/19035693/full_citation/Rhombencephalosynapsis_associated_with_autosomal_dominant_polycystic_kidney_disease_Type_1_Elliott R, Harter DH 
Rhombencephalosynapsis associated with autosomal dominant polycystic kidney disease Type 1. [JOURNAL ARTICLE]
J Neurosurg Pediatrics 2008 Dec; 2(6):435-437.
Abstract | Full CitationSonographic Diagnosis of an Unusual Case of Multilocular Cystic Nephroma Mimicking Polycystic Kidney Disease.http://www.unboundmedicine.com/medline/ebm/record/19034827/full_citation/Sonographic_Diagnosis_of_an_Unusual_Case_of_Multilocular_Cystic_Nephroma_Mimicking_Polycystic_Kidney_Disease_Deeg KH, Gerdemann C, Weingärtner K, et al. 
Sonographic Diagnosis of an Unusual Case of Multilocular Cystic Nephroma Mimicking Polycystic Kidney Disease. [JOURNAL ARTICLE]
Ultraschall Med 2008 Nov 25.
Abstract | Full Citation | Find Related Articles Matrix proteins of basement membrane of intrahepatic bile ducts are degraded in congenital hepatic fibrosis and Caroli's disease.http://www.unboundmedicine.com/medline/ebm/record/19025978/full_citation/Matrix_proteins_of_basement_membrane_of_intrahepatic_bile_ducts_are_degraded_in_congenital_hepatic_fibrosis_and_Caroli's_disease_Yasoshima M, Sato Y, Furubo S, et al. 
Matrix proteins of basement membrane of intrahepatic bile ducts are degraded in congenital hepatic fibrosis and Caroli's disease. [JOURNAL ARTICLE]
J Pathol 2008 Oct 16.
Abstract | Full CitationGenomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencing.http://www.unboundmedicine.com/medline/ebm/record/19023858/full_citation/Genomic_deletions_of_OFD1_account_for_23_of_oral_facial_digital_type_1_syndrome_after_negative_DNA_sequencing_Thauvin-Robinet C, Franco B, Saugier-Veber P, et al. 
Genomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencing. [JOURNAL ARTICLE]
Hum Mutat 2008 Nov 19.
Abstract | Full CitationPseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease.http://www.unboundmedicine.com/medline/ebm/record/19021639/full_citation/Pseudoexon_activation_in_the_PKHD1_gene:_a_French_founder_intronic_mutation_IVS46+653A>G_causing_severe_autosomal_recessive_polycystic_kidney_disease_Michel-Calemard L, Dijoud F, Till M, et al. 
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease. [JOURNAL ARTICLE]
Clin Genet 2008 Nov 17.
Full Citation | Find Related Articles [Bardet-Biedl syndrome.]http://www.unboundmedicine.com/medline/ebm/record/19019343/full_citation/[Bardet_Biedl_syndrome_]Rooryck C, Lacombe D 
[Bardet-Biedl syndrome.] [JOURNAL ARTICLE]
Ann Endocrinol (Paris) 2008 Nov 17.
Abstract | Full CitationSpontaneous spinal cerebrospinal fluid leak as a cause of coma after craniotomy for clipping of an unruptured intracranial aneurysm.http://www.unboundmedicine.com/medline/ebm/record/19012477/full_citation/Spontaneous_spinal_cerebrospinal_fluid_leak_as_a_cause_of_coma_after_craniotomy_for_clipping_of_an_unruptured_intracranial_aneurysm_Schievink WI, Palestrant D, Maya MM, et al. 
Spontaneous spinal cerebrospinal fluid leak as a cause of coma after craniotomy for clipping of an unruptured intracranial aneurysm. [JOURNAL ARTICLE]
J Neurosurg 2008 Nov 14.
Abstract | Full Citation | Publisher Full Text | Find Related Articles