Found: 17
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Endoscopic Findings and Correlation with Outcome in Oesophagal Battery Button Ingestion in Children.
- Published in:
- Pakistan Armed Forces Medical Journal, 2024, v. 74, n. 2, p. 549, doi. 10.51253/pafmj.v74i2.9601
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- Article
Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani Children.
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- Turkish Journal of Gastroenterology, 2023, v. 34, n. 10, p. 1088, doi. 10.5152/tjg.2023.22791
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- Article
The mutational landscape of genetic cholestatic diseases in Pakistani children.
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- Journal of the Pakistan Medical Association, 2023, v. 73, n. 8, p. 1610, doi. 10.47391/JPMA.7069
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- Article
Assessment of Quality of Life Among Children with Inflammatory Bowel Disease.
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- Pakistan Armed Forces Medical Journal, 2022, v. 72, n. 5, p. 1698, doi. 10.51253/pafmj.v72i5.6845
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- Article
Spectrum of clinical manifestation of methylmalonic acidemia and homocystinuria in a family of six siblings: novel combination of transcobalamin receptor defect (CD320) and cblC deficiency (MMACHC)
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- Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00197-2
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- Article
Spectrum of clinical manifestation of methylmalonic acidemia and homocystinuria in a family of six siblings: novel combination of transcobalamin receptor defect (CD320) and cblC deficiency (MMACHC).
- Published in:
- Egyptian Journal of Medical Human Genetics, 2021, v. 22, p. 1, doi. 10.1186/s43042-021-00197-2
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- Article
Very early onset inflammatory bowel disease: Spectrum of clinical presentation, diagnostic tools and outcome in children.
- Published in:
- Journal of the Pakistan Medical Association, 2021, v. 71, n. 10, p. 2350, doi. 10.47391/JPMA.05-725
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- Article
Chanarin–Dorfman syndrome: clinical/genetic features and natural history in six Pakistani patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00189-2
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- Article
Variability of clinical and biochemical phenotype in liver phosphorylase kinase deficiency with variants in the phosphorylase kinase (PHKG2) gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 9, p. 1117, doi. 10.1515/jpem-2019-0603
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- Article
Complicated gastric duplication cyst presenting as cystic intraperitoneal collection: a case report.
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- Annals of Pediatric Surgery, 2020, v. 16, n. 1, p. 1, doi. 10.1186/s43159-020-00063-7
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- Article
HEPATIC GLYCOGENOSIS IN CHILDREN: SPECTRUM OF PRESENTATION AND DIAGNOSTIC MODALITIES.
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- Journal of Ayub Medical College Abbottabad - Pakistan, 2019, v. 31, n. 3, p. 368
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- Article
Is Hepatovenocaval Syndrome a Different Entity from Budd-Chiari Syndrome in Children?
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- Journal of the College of Physicians & Surgeons Pakistan, 2018, v. 28, n. 5, p. 344, doi. 10.29271/jcpsp.2018.05.1.344
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- Article
Berardinelli-Seip Congenital Generalised Lipodystrophy.
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- Journal of the College of Physicians & Surgeons Pakistan, 2018, v. 28, n. 5, p. 406, doi. 10.29271/jcpsp.2018.05.406
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- Article
Mucopolysaccharidoses -- Clinical Spectrum and Frequency of Different Types.
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- Journal of the College of Physicians & Surgeons Pakistan, 2017, v. 27, n. 2, p. 80
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- Article
Chanarin-Dorfman Syndrome.
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- Journal of the College of Physicians & Surgeons Pakistan, 2016, v. 26, n. 9, p. 787
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- Article
Congenital hepatic fibrosis: clinical presentation, laboratory features and management at a tertiary care hospital of Lahore.
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- Journal of the Pakistan Medical Association, 2016, v. 66, n. 8, p. 984
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- Article
Spectrum of Inherited Metabolic Disorders in Pakistani Children Presenting at a Tertiary Care Centre.
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- Journal of the College of Physicians & Surgeons Pakistan, 2016, v. 26, n. 6, p. 498
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- Article