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Clinical Nephrology. Case Studies
|
April 23, 2020
Eculizumab in chemotherapy-induced thrombotic microangiopathy
Lena Schulte-Kemna, Barbara Reister, Lucas Bettac, et al.
Diabetes Care
|
March 6, 2007
Digenic inheritance of hepatocyte nuclear factor-1alpha and -1beta with maturity-onset diabetes of the young, polycystic thyroid, and urogenital malformations
Beate Karges, Carsten Bergmann, Katrina Scholl, et al.
International Journal of Molecular Sciences
|
January 27, 2024
Congenital Hyperinsulinism in Humans and Insulin Secretory Dysfunction in Mice Caused by Biallelic <i>DNAJC3</i> Variants
Alena Welters, Oliver Nortmann, Laura Wörmeyer, et al.
Human Molecular Genetics
|
January 30, 2003
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15
Jan Senderek, Carsten Bergmann, Susanne Weber, et al.
Urolithiasis
|
February 25, 2019
Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting
Ria Schönauer, Friederike Petzold, Wilhelmina Lucinescu, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
April 16, 2013
Combined liver-kidney transplantation for children with autosomal recessive polycystic kidney disease (ARPKD): indication and outcome
Florian Brinkert, Anja Lehnhardt, Carmen Montoya, et al.
Experimental Dermatology
|
March 24, 2011
Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations
Carsten Bergmann, Marion Wobser, Henner Morbach, et al.
Kidney International
|
August 26, 2011
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies
Moumita Chaki, Julia Hoefele, Susan J Allen, et al.
Clinical Kidney Journal
|
August 11, 2018
Membranoproliferative glomerulonephritis and C3 glomerulopathy in children: change in treatment modality? A report of a case series
Giuseppina Spartà, Ariana Gaspert, Thomas J Neuhaus, et al.
Kidney & Blood Pressure Research
|
May 13, 2010
The mTOR pathway is activated in human autosomal-recessive polycystic kidney disease
Jan Ulrich Becker, Anabelle Opazo Saez, Klaus Zerres, et al.
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of 23
Search research articles
Search
Showing results (81-90 of 228) with videos related to
Sort By:
Page
of 23
Clinical Nephrology. Case Studies
|
April 23, 2020
Eculizumab in chemotherapy-induced thrombotic microangiopathy
Lena Schulte-Kemna, Barbara Reister, Lucas Bettac, et al.
Diabetes Care
|
March 6, 2007
Digenic inheritance of hepatocyte nuclear factor-1alpha and -1beta with maturity-onset diabetes of the young, polycystic thyroid, and urogenital malformations
Beate Karges, Carsten Bergmann, Katrina Scholl, et al.
International Journal of Molecular Sciences
|
January 27, 2024
Congenital Hyperinsulinism in Humans and Insulin Secretory Dysfunction in Mice Caused by Biallelic <i>DNAJC3</i> Variants
Alena Welters, Oliver Nortmann, Laura Wörmeyer, et al.
Human Molecular Genetics
|
January 30, 2003
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15
Jan Senderek, Carsten Bergmann, Susanne Weber, et al.
Urolithiasis
|
February 25, 2019
Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting
Ria Schönauer, Friederike Petzold, Wilhelmina Lucinescu, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
April 16, 2013
Combined liver-kidney transplantation for children with autosomal recessive polycystic kidney disease (ARPKD): indication and outcome
Florian Brinkert, Anja Lehnhardt, Carmen Montoya, et al.
Experimental Dermatology
|
March 24, 2011
Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations
Carsten Bergmann, Marion Wobser, Henner Morbach, et al.
Kidney International
|
August 26, 2011
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies
Moumita Chaki, Julia Hoefele, Susan J Allen, et al.
Clinical Kidney Journal
|
August 11, 2018
Membranoproliferative glomerulonephritis and C3 glomerulopathy in children: change in treatment modality? A report of a case series
Giuseppina Spartà, Ariana Gaspert, Thomas J Neuhaus, et al.
Kidney & Blood Pressure Research
|
May 13, 2010
The mTOR pathway is activated in human autosomal-recessive polycystic kidney disease
Jan Ulrich Becker, Anabelle Opazo Saez, Klaus Zerres, et al.
Page
of 23