Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2369

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman ; volume:21 ; number:1 ; day:14 ; month:8 ; year:2020 ; pages:1-11 ; date:12.2020
BMC nephrology ; 21, Heft 1 (14.8.2020), 1-11, 12.2020

Creator: Alawi, Intisar Al
Molinari, Elisa
Salmi, Issa Al
Rahbi, Fatma Al
Mawali, Adhra Al
Sayer, John A.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12882-020-02013-2

URN: urn:nbn:de:101:1-2020100723234796451423

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:57 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Alawi, Intisar Al
Molinari, Elisa
Salmi, Issa Al
Rahbi, Fatma Al
Mawali, Adhra Al
Sayer, John A.
SpringerLink (Online service)

Other Objects (12)

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Konferenzschrift | Kongress

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Konferenzschrift | Kongress

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Konferenzschrift | Kongress

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Early clinical management of autosomal recessive polycystic kidney disease

Genetics of autosomal recessive polycystic kidney disease and its differential diagnoses

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension

Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease : 39 tables

Autosomal dominant polycystic kidney disease in Colombia

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive cerebellar ataxias

Related objects

Reset password