S. A. Paracha

发表

THE IMPACT OF ANATOMICAL VARIATION OF LOWER POLE COLLECTING SYSTEM OF KIDNEY ON STONE FORMATION

Z. Shah, Abdul Sahib Khan, S. A. Paracha, 2012 .

COLLECTING SYSTEM OF KIDNEY ON STONE FORMA COLLECTING SYSTEM OF KIDNEY ON STONE FORMA COLLECTING SYSTEM OF KIDNEY ON STONE FORMA COLLECTING SYSTEM OF KIDNEY ON STONE FORMA COLLECTING SYSTEM OF KIDNEY ON STONE FORMATION

Z. Shah, Abdul Sahib Khan, S. A. Paracha, 2012 .

OUTCOME OF OPEN VERSUS CLOSED SURGICAL TECHNIQUE FOR TREATMENT OF CHRONIC PILONIDAL SINUS: A RANDOMIZED CONTROL TRIAL

S. A. Paracha, Mohammad Tahir, Sayed Zulfiqar Ali Shah, 2013 .

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

D. Misceo, S. Antonarakis, S. Riazuddin, 2017, Genetics in Medicine.

Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature

S. Antonarakis, A. Serretti, E. Falconnet, 2018, Human molecular genetics.

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees

S. Antonarakis, Inayat Shah, A. Nazir, 2023, Genes.

Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature.

S. Antonarakis, E. Krüger, V. Zoete, 2020, Human molecular genetics.

Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.

S. Antonarakis, E. Falconnet, H. Bellen, 2019, American journal of human genetics.

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

A. Reymond, S. Antonarakis, H. Darvish, 2021, npj Genomic Medicine.

Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features.

S. Antonarakis, E. Falconnet, N. Katsanis, 2019, American journal of human genetics.

De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.

R. Pfundt, C. Cytrynbaum, J. Vincent, 2020, American journal of human genetics.

Drug-Resistant Proteus Virulence Factors Characterization and Their Inhibition Using Probiotic Bacteria

N. Akbar, S. A. Paracha, Sadir Zaman, 2022, Jundishapur Journal of Microbiology.

GROSS PYURIC DIABETICS WITH UNCONTROLLED GLYCEMIA: PATTERN OF PATHOGENIC ORGANISMS AND ANTIMICROBIAL SUSCEPTIBILITY

Syed Fahim Shah, S. A. Paracha, 2016 .

ROLE OF ILEOSTOMY IN THE MANAGEMENT OF LATE CASES OF TYPHOID INTESTINAL PERFORATION

M. Tahir, S. A. Paracha, Qazi Tahir Uddin, 2012 .

ANATOMICAL VARIATIONS OF CYSTIC DUCT ENCOUNTERED DURING OPEN CHOLECYSTECTOMY

Abdul Sahib Khan, S. A. Paracha, Khizar Wahab, 2012 .

OUTCOME OF DARN REPAIR WITH POLYPROPYLENE FOR PRIMARY INGUINAL HERNIA: AN EXPERIENCE OF 837 CASES

I. Khan, M. Nasir, S. A. Paracha, 2013 .

Luminal Diameters of Major Coronary Arteries

Shemaila Saleem, S. A. Paracha, Q. W. Ullah, 2013 .

FOXI3 pathogenic variants cause one form of craniofacial microsomia

J. Lupski, Xiaogang Wang, S. Antonarakis, 2023, Nature Communications.

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

D. Misceo, S. Antonarakis, S. Riazuddin, 2018, Genetics in Medicine.

Success of 14-day triple and quadruple therapy for the control of Helicobacter pylori infections in Kohat district

M. Hussain, Syed Fahim Shah, S. A. Paracha, 2022, Drug target insights.

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome

S. Khan, Q. Alam, Shazia Khan, 2023, Genes.

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

A. Reymond, S. Antonarakis, H. Darvish, 2021, npj Genomic Medicine.

Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency.

S. Antonarakis, C. Pournaras, C. Rivolta, 2019, Human molecular genetics.