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Tahir Shaheen
Tahir Shaheen
Medicine
Internal medicine
Endocrinology
Mutation (genetic algorithm)
Physical therapy
5
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2024
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Clinical spectrum of congenital adrenal hyperplasia due to 3 beta hydroxysteroid dehydrogenase deficiency; A case series
2021
Tahir Shaheen
Sommayya Aftab
Muhammad Nadeem
Anjum Saeed
Huma Arshad
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Clinical Spectrum of Hypomagnesemia type 1 (HOMG1) due to Novel TRPM6 mutations
2021
Sommayya Aftab
Muhammad Nadeem Anjum
Anjum Saeed
Tahir Shaheen
Huma Arshad Cheema
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Lack of Cinacalcet response in Neonatal Severe Hyperparathyroidism (NSHPT) due to homozygous CASR mutation
2021
Ammar Haider
Sommayya Aftab
Shumaila Chaudhary
Mazhar Qadir
Anjum Muhammad Nadeem
Anjum Saeed
Tahir Shaheen
Farah Haroon
Cheema Huma Arshad
Mehmood Shaukat
Khawaja Ahmad
Irfan Waheed
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Diagnostic Challenges of Vitamin D-Dependent Rickets Type 1A (VDDR1A) caused by CYP27B1 mutation in Resource Limited Countries: A Case Series from Three families
2021
Sommayya Aftab
Tahir Shaheen
Anjum Muhammad Nadeem
Ahmed Imran
Anjum Saeed
Qureshi Abid Ali
Huma Arshad Cheema
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Bradycardia and pacemakers
2020
Innovait
Mohammed Sohail Ahmed
Tahir Shaheen
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