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Farkhanda Hafeez

Showing results (11-20 of 14) with videos related to

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Journal of Ayub Medical College, Abbottabad : JAMC|March 24, 2016
TACROLIMUS DRUG LEVEL AND RESPONSE TO TREATMENT IN IDIOPATHIC CHILDHOOD STEROID RESISTANT NEPHROTIC SYNDROMESyed Sajid Hussain Shah, Farkhanda Hafeez, Naureen Akhtar
Gene|May 9, 2012
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from PakistanAiysha Abid, Shagufta Khaliq, Saba Shahid, et al.
Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Genes & Diseases|June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletionsKonstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Ayub Medical College, Abbottabad : JAMC|March 24, 2016
TACROLIMUS DRUG LEVEL AND RESPONSE TO TREATMENT IN IDIOPATHIC CHILDHOOD STEROID RESISTANT NEPHROTIC SYNDROMESyed Sajid Hussain Shah, Farkhanda Hafeez, Naureen Akhtar
Gene|May 9, 2012
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from PakistanAiysha Abid, Shagufta Khaliq, Saba Shahid, et al.
Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Genes & Diseases|June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletionsKonstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
Pageof 2