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A case of multisystem inflammatory syndrome in children presenting as systemic onset juvenile idiopathic arthritis

Journal of the Pakistan Medical Association, 2022-01, Vol.72 (1), p.161

2022

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Frequency of vitamin D deficiency in children with iron deficiency anaemia and factors associated with vitamin D deficiency

Journal of the Pakistan Medical Association, 2024-04, Vol.74 (4), p.626-630

2024

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Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome

Medicina (Kaunas, Lithuania), 2022-12, Vol.58 (12), p.1784

2022

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Whole exome sequencing identified a novel splice donor site variant in interleukin 2 receptor alpha chain

Immunogenetics (New York), 2023-04, Vol.75 (2), p.71-79

2023

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EPA-0938 - Psychiatric comorbidity among individuals with substance dependence at a tertiary care hospital in Pakistan

European psychiatry, 2014, Vol.29, p.1-1

2014

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Time to return back the soul of science

Journal of Pakistan Psychiatric Society, 2021-11, Vol.18 (2), p.5-6

2021

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Integrity shots; contemporary indigenous research to reconcile with standards (part 2)

Journal of Pakistan Psychiatric Society, 2021-03, Vol.18 (1), p.5-6

2021

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Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations

Molecular biology reports, 2024-12, Vol.51 (1), p.573-573, Article 573

2024

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Epidemiology and clinical spectrum of pediatric patients with human immunodeficiency virus (HIV) infection: A 15 years' experience

Pakistan journal of medical sciences, 2023-06, Vol.39 (3), p.820-824

2023

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Mutational analysis in different genes underlying severe combined immunodeficiency in seven consanguineous Pakistani families

Molecular biology reports, 2024-12, Vol.51 (1), p.302-302, Article 302

2024

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Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia

The journal of gene medicine, 2024-01, Vol.26 (1), p.e3601-n/a

2024

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A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorder

Neurogenetics, 2022-07, Vol.23 (3), p.203-212

2022

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Frequency, causes and outcome of neonates with respiratory distress admitted to Neonatal Intensive Care Unit, National Institute of Child Health, Karachi

Journal of the Pakistan Medical Association, 2015-07, Vol.65 (7), p.771-775

2015

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Frequency of hyponatraemia and hypokalaemia in malnourished children with acute diarrhoea

Journal of the Pakistan Medical Association, 2016-09, Vol.66 (9), p.1077-1080

2016

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Frequency of acute bacterial meningitis in children with first episode of febrile seizures

Journal of the Pakistan Medical Association, 2017-07, Vol.67 (7), p.1054-1058

2017

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COMPARISON OF EFFICACY OF YOGURT VERSUS PROBIOTICS FOR THE MANAGEMENT OF ACUTE DIARRHOEA

Journal of Ayub Medical College, Abbottabad, 2022-04, Vol.34 (2)

2022

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EXTENSIVELY DRUG-RESISTANT ENTERIC FEVER IN CHILDREN: SURGING THREATS OF ANTIMICROBIAL RESISTANCE AND POSSIBLE SOLUTIONS

Journal of Ayub Medical College, Abbottabad, 2023-07, Vol.35 (3)

2023

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Risk factors for mortality among admitted children with complications of measles in Pakistan: An observational study

Journal of the Pakistan Medical Association, 2021-02, Vol.71 (2(A)), p.497-501

2021

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Risk factors for mortality among admitted children with complications of measles in Pakistan – an observational

Journal of the Pakistan Medical Association, 2020-11, p.1-14

2020

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Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis

Clinical and experimental dermatology, 2022-06, Vol.47 (6), p.1137-1143

2022

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Sequence variants in three genes underlying leukodystrophy in Pakistani families

International journal of developmental neuroscience, 2020-08, Vol.80 (5), p.380-388

2020

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Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion

International journal of developmental neuroscience, 2022-12, Vol.82 (8), p.789-805

2022

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Clinical and genetic characterization of congenital lipoid adrenal hyperplasia

Clinical dysmorphology, 2020-10, Vol.29 (4), p.173-176

2020

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Etiological Spectrum of Lymphadenopathy Among Children on Lymph Node Biopsy

Curēus (Palo Alto, CA), 2024-08

2024

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Exome Sequencing Revealed a Novel Splice Site Variant in the ICRB2/I Gene Underlying Nephrotic Syndrome

Medicina (Kaunas, Lithuania), 2022-12, Vol.58 (12)

2022

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A case of multisystem inflammatory syndrome in children presenting as systemic onset juvenile idiopathic arthritis

Frequency of vitamin D deficiency in children with iron deficiency anaemia and factors associated with vitamin D deficiency

Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome

Whole exome sequencing identified a novel splice donor site variant in interleukin 2 receptor alpha chain

EPA-0938 - Psychiatric comorbidity among individuals with substance dependence at a tertiary care hospital in Pakistan

Time to return back the soul of science

Integrity shots; contemporary indigenous research to reconcile with standards (part 2)

Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations

Epidemiology and clinical spectrum of pediatric patients with human immunodeficiency virus (HIV) infection: A 15 years' experience

Mutational analysis in different genes underlying severe combined immunodeficiency in seven consanguineous Pakistani families

Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia

A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorder

Frequency, causes and outcome of neonates with respiratory distress admitted to Neonatal Intensive Care Unit, National Institute of Child Health, Karachi

Frequency of hyponatraemia and hypokalaemia in malnourished children with acute diarrhoea

Frequency of acute bacterial meningitis in children with first episode of febrile seizures

COMPARISON OF EFFICACY OF YOGURT VERSUS PROBIOTICS FOR THE MANAGEMENT OF ACUTE DIARRHOEA

EXTENSIVELY DRUG-RESISTANT ENTERIC FEVER IN CHILDREN: SURGING THREATS OF ANTIMICROBIAL RESISTANCE AND POSSIBLE SOLUTIONS

Risk factors for mortality among admitted children with complications of measles in Pakistan: An observational study

Risk factors for mortality among admitted children with complications of measles in Pakistan – an observational

Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis

Sequence variants in three genes underlying leukodystrophy in Pakistani families

Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion

Clinical and genetic characterization of congenital lipoid adrenal hyperplasia

Etiological Spectrum of Lymphadenopathy Among Children on Lymph Node Biopsy

Exome Sequencing Revealed a Novel Splice Site Variant in the ICRB2/I Gene Underlying Nephrotic Syndrome

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