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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|
September 9, 2004
Management of gestational trophoblastic tumours: a five-year clinical experience
Bushra Rauf, Lubna Hassan, Shafiq Ahmed
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|
October 2, 2007
External cephalic version for breech presentation at term
Bushra Rauf, Mehrun- Nisa, Lubna Hassan
Bjpsych Open
|
March 19, 2021
COVID-19-related prescribing challenge in intellectual disability
Bushra Rauf, Hafsa Sheikh, Hassan Majid, et al.
Endocrine
|
September 28, 2022
Treatment with combined resveratrol and myoinositol ameliorates endocrine, metabolic alterations and perceived stress response in women with PCOS: a double-blind randomized clinical trial
Sehresh Hassan, Mohsin Shah, Muhammad Omar Malik, et al.
Molecular Vision
|
March 14, 2020
Novel mutations in <i>LTBP2</i> identified in familial cases of primary congenital glaucoma
Bushra Rauf, Bushra Irum, Shahid Y Khan, et al.
Human Genome Variation
|
August 11, 2016
A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Bushra Rauf, Bushra Irum, Firoz Kabir, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
January 23, 2025
Comparative efficacy of combined myo-inositol and D-chiro inositol versus metformin across PCOS Phenotypes: enhancing ovarian function, ovulation, and stress response in a prospective clinical trial
Meena Gul, Hina Khan, Bushra Rauf, et al.
Human Genome Variation
|
September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts
Bushra Irum, Firoz Kabir, Nadav Shoshany, et al.
Advances in Therapy
|
May 28, 2021
Acetyl-L-Carnitine Ameliorates Metabolic and Endocrine Alterations in Women with PCOS: A Double-Blind Randomized Clinical Trial
Saman Tauqir, Momina Israr, Bushra Rauf, et al.
Human Genome Variation
|
May 16, 2020
Mutations in <i>CERKL</i> and <i>RP1</i> cause retinitis pigmentosa in Pakistani families
Raheela Nadeem, Firoz Kabir, Jiali Li, et al.
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of 2
Search research articles
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Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|
September 9, 2004
Management of gestational trophoblastic tumours: a five-year clinical experience
Bushra Rauf, Lubna Hassan, Shafiq Ahmed
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|
October 2, 2007
External cephalic version for breech presentation at term
Bushra Rauf, Mehrun- Nisa, Lubna Hassan
Bjpsych Open
|
March 19, 2021
COVID-19-related prescribing challenge in intellectual disability
Bushra Rauf, Hafsa Sheikh, Hassan Majid, et al.
Endocrine
|
September 28, 2022
Treatment with combined resveratrol and myoinositol ameliorates endocrine, metabolic alterations and perceived stress response in women with PCOS: a double-blind randomized clinical trial
Sehresh Hassan, Mohsin Shah, Muhammad Omar Malik, et al.
Molecular Vision
|
March 14, 2020
Novel mutations in <i>LTBP2</i> identified in familial cases of primary congenital glaucoma
Bushra Rauf, Bushra Irum, Shahid Y Khan, et al.
Human Genome Variation
|
August 11, 2016
A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Bushra Rauf, Bushra Irum, Firoz Kabir, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
January 23, 2025
Comparative efficacy of combined myo-inositol and D-chiro inositol versus metformin across PCOS Phenotypes: enhancing ovarian function, ovulation, and stress response in a prospective clinical trial
Meena Gul, Hina Khan, Bushra Rauf, et al.
Human Genome Variation
|
September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts
Bushra Irum, Firoz Kabir, Nadav Shoshany, et al.
Advances in Therapy
|
May 28, 2021
Acetyl-L-Carnitine Ameliorates Metabolic and Endocrine Alterations in Women with PCOS: A Double-Blind Randomized Clinical Trial
Saman Tauqir, Momina Israr, Bushra Rauf, et al.
Human Genome Variation
|
May 16, 2020
Mutations in <i>CERKL</i> and <i>RP1</i> cause retinitis pigmentosa in Pakistani families
Raheela Nadeem, Firoz Kabir, Jiali Li, et al.
Page
of 2