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Search Results - Wali, Ansar A
Search Results - Wali, Ansar A
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Orbital SOX10-mutant schwannoma with plexiform growth: Expanding the histopathological spectrum of a new molecular group
by
Wali, Ansar A
,
Yang, Robin
,
Merbs, Shannath L
,
Rodriguez, Fausto J
,
Eberhart, Charles G
,
Lucas, Calixto-Hope G
Published in
Journal of neuropathology and experimental neurology
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Ethnomedicinal appraisal of plants used for the treatment of gastrointestinal complaints by tribal communities living in Diamir district, Western Himalayas, Pakistan
by
Wali, Rahmat
,
Khan, Muhammad Faraz
,
Mahmood, Ansar
,
Mahmood, Majid
,
Qureshi, Rahmatullah
,
Ahmad, Khawaja Shafique
,
Mashwani, Zia-Ur-Rehman
Published in
PloS one
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Ameliorative effects of Cuscuta reflexa and Peucedanum grande on letrozole induced polycystic ovary syndrome in Wistar rats
by
Kausar, Firdaus
,
Rather, Muzafar Ahmad
,
Bashir, Showkeen Muzamil
,
Alsaffar, Rana M.
,
Nabi, Showkat ul
,
Ali, Sofi Imtiyaz
,
Goswami, Pankaj
,
Ahmad, Ansar
,
Rashid, Summya
,
Wali, Adil Farooq
Published in
Redox report : communications in free radical research
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99mTc-Tilmanocept vs. Sulfur Colloid for Sentinel Node Biopsy for Melanoma in the Head and Neck
by
Sayal, Navdeep R.
,
Schafer, Jeffrey
,
Jayne, Christopher
,
Wali, Ansar
,
Lindau, Robert
,
Sayles, Harlan
,
Marr, Alissa
,
Aurit, Sarah
,
Lydiatt, William
,
Holcomb, Andrew
,
Militsakh, Oleg
,
Coughlin, Andrew
,
Osmolak, Angela
,
Panwar, Aru
Published in
Indian journal of surgical oncology
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Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome
by
Ali, Ghazanfar
,
Sadia
,
Foo, Jia Nee
,
Nasir, Abdul
,
Chang, Chu-Hua
,
Chew, Elaine GuoYan
,
Latif, Zahid
,
Azeem, Zahid
,
Ain-ul-Batool, Syeda
,
Kazmi, Syed Akif Raza
,
Awan, Naheed Bashir
,
Khan, Abdul Hameed
,
Rehman, Fazal-Ur
,
Khalid, Madiha
,
Wali, Abdul
,
Sarwar, Samina
,
Akhtar, Wasim
,
Ahmed Abbasi, Ansar
,
Nisar, Rameez
Published in
BioMed research international
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ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment
by
Bharadwaj, Thashi
,
Schrauwen, Isabelle
,
Rehman, Sakina
,
Liaqat, Khurram
,
Acharya, Anushree
,
Giese, Arnaud P J
,
Nouel-Saied, Liz M
,
Nasir, Abdul
,
Everard, Jenna L
,
Pollock, Lana M
,
Zhu, Shaoyuan
,
Bamshad, Michael J
,
Nickerson, Deborah A
,
Ali, Raja Hussain
,
Ullah, Asmat
,
Wali, Abdul
,
Ali, Ghazanfar
,
Santos-Cortez, Regie Lyn P
,
Ahmed, Zubair M
,
McDermott, Jr, Brian M
,
Ansar, Muhammad
,
Riazuddin, Saima
,
Ahmad, Wasim
,
Leal, Suzanne M
Published in
European journal of human genetics : EJHG
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99m Tc-Tilmanocept vs. Sulfur Colloid for Sentinel Node Biopsy for Melanoma in the Head and Neck
by
Sayal, Navdeep R
,
Schafer, Jeffrey
,
Jayne, Christopher
,
Wali, Ansar
,
Lindau, Robert
,
Sayles, Harlan
,
Marr, Alissa
,
Aurit, Sarah
,
Lydiatt, William
,
Holcomb, Andrew
,
Militsakh, Oleg
,
Coughlin, Andrew
,
Osmolak, Angela
,
Panwar, Aru
Published in
Indian journal of surgical oncology
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Ethnomedicinal appraisal of plants used for the treatment of gastrointestinal complaints by tribal communities living in Diamir district, Western Himalayas, Pakistan
by
Rahmat Wali
,
Muhammad Faraz Khan
,
Ansar Mahmood
,
Majid Mahmood
,
Rahmatullah Qureshi
,
Khawaja Shafique Ahmad
,
Zia-ur-Rehman Mashwani
Published in
PloS one
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Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis
by
Ali, Raja Hussain
,
Mahmood, Sabba
,
Raza, Syed Irfan
,
Aziz, Abdul
,
Irfanullah
,
Naqvi, Syed Kamran-ul-Hassan
,
Wasif, Naveed
,
Ansar, Muhammad
,
Ahmad, Wasim
,
Shah, Sayed Hajan
,
Khan, Bakht Tarin
,
Zaman, Qaiser
,
Gul, Ajab
,
Wali, Abdul
,
Ali, Ghazanfar
,
Khan, Saadulah
,
Khisroon, Muhammad
,
Basit, Sulman
Published in
Journal of dermatological science
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Mutation Analysis of the ASPM Gene in 18 Pakistani Families With Autosomal Recessive Primary Microcephaly
by
Kousar, Rizwana
,
Nawaz, Hira
,
Khurshid, Maryam
,
Ali, Ghazanfer
,
Khan, Saad Ullah
,
Mir, Hina
,
Ayub, Muhammad
,
Wali, Abdul
,
Ali, Nadir
,
Jelani, Musharraf
,
Basit, Sulman
,
Ahmad, Wasim
,
Ansar, Muhammad
Published in
Journal of child neurology
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Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia
by
Azeem, Zahid
,
Naqvi, Syed Kamran-Ul-Hassan
,
Ansar, Muhammad
,
Wali, Abdul
,
Naveed, Abdul Khaliq
,
Ali, Ghazanfar
,
Hassan, Muhammad Jawad
,
Tariq, Muhammad
,
Basit, Sulman
,
Ahmad, Wasim
Published in
Archives of Dermatological Research
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