Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Samer Sikander"'
Autor:
Muhammad Umar Nisar, Nisar Ahmed Khan, Noshela Javed, Samer Sikander, Muhammad Amjad Chaudhry, Ali Raza Chaudhry
Publikováno v:
Pakistan Journal of Medical Research, Vol 58, Iss 4 (2020)
Background: Esophageal Atresia (EA) with or without associated tracheo-esophageal fistula (TEF) is one of the common congenital anomaly that can be life threatening if left unattended. In low and middle income countries like Pakistan, the management
Externí odkaz:
https://doaj.org/article/4a20554167f2461791f1e646f1b5ebf2
Autor:
Muhammad Umar Nisar, Samer Sikander, Nadeem Akhtar, Quratulain Arshad, Maryam Nisar, Mehr-un-Nisa Shahid Baig
Publikováno v:
Journal of Neonatal Surgery, Vol 8, Iss 2 (2019)
Please see fulltext
Externí odkaz:
https://doaj.org/article/8773513d896647b3927c9294258f4ea0
FAMILIAL CAMPTODACTYLY COXA VARA PERICARDITIS SYNDROME MASQUARADING AS JUVUNILE IDIOPATHIC ARTHRITIS
Publikováno v:
Khyber Medical University Journal, Vol 10, Iss 4, Pp 221-223 (2018)
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is a rare autosomal recessive disease characterized by congenital or early-onset camptodactyly, childhood-onset non-inflammatory arthropathy associated with synovial hyperplasia, co
Externí odkaz:
https://doaj.org/article/2e4e70fd7a494dbf94b5d5c32c194117
Autor:
Ali Raza Chaudhry, Muhammad Umar Nisar, Samer Sikander, Nadeem Akhtar, Nisar Khan, Anwar Khan
Publikováno v:
Journal of Saidu Medical College, Swat. 11:39-44
Background: Intestinal obstruction in children is a very common cause of admission in hospitals with usually a high mortality andmorbidity rate. There is a geographical variability in patterns of intestinal obstruction in pediatric population around
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::897a2144dfc0e78c5eec8f1f61e343c4
https://doi.org/10.52206/jsmc.2021.11.1.39-44
https://doi.org/10.52206/jsmc.2021.11.1.39-44
Publikováno v:
Journal of Pediatric and Adolescent Surgery. 1:117-119
Background: Congenital epulis is a rare benign, smooth, sessile, or pedunculated, solitary mass of varying sizes commonly occurring at the anterior alveolar ridge of the maxilla. It can occur as a solitary as well as a multifocal lesion. Case Present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d54a7a2a17b912c07b9f6575147b6f5
https://doi.org/10.46831/jpas.v1i2.99
https://doi.org/10.46831/jpas.v1i2.99
Autor:
Muhammad Amjad Chaudhry, Muhammad Umar Nisar, Sadia Asmat Burki, Samer Sikander, Asad Iqbal, Noshela Javed
Publikováno v:
Journal of Pediatric and Adolescent Surgery. 1
Background: The survival and outcome of neonates with anorectal malformations (ARM) have much improved in the developed countries due to optimal perioperative and postoperative care but in developing countries, sepsis, low birth weight, delayed prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::869835b89b96fbc632108114a188e0ca
https://doi.org/10.46831/jpas.v1i2.30
https://doi.org/10.46831/jpas.v1i2.30
Autor:
Muhammad Umar, Nisar, Samer, Sikander, Nisar Ahmed, Khan, Noshela, Javed, Muhammad Amjad, Chaudhary, Mohammed Abdulmomen, Abdullah Saif
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 32(1)
Intussusception is an acute surgical emergency and one of the most common causes of acute abdomen in early paediatric age group with peak incidence between 3 months to 3 years. It is considered the most common cause of intestinal obstruction in first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa313e158041d9ebb34fbbfd762e6fed
https://pubmed.ncbi.nlm.nih.gov/32468746
https://pubmed.ncbi.nlm.nih.gov/32468746
Publikováno v:
Journal of the College of Physicians and Surgeons Pakistan. 29:S45-S47
Iliopsoas abscess (IPA) is rare in children but exceptional in neonates. Fewer than 30 cases have been reported in literature. We present a case of 11-day neonate who was brought with left inguinal swelling along with significantly raised white cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4559c9432f8d4b9d67d4555a13b3e0b
https://doi.org/10.29271/jcpsp.2019.06.s45
https://doi.org/10.29271/jcpsp.2019.06.s45
FAMILIAL CAMPTODACTYLY COXA VARA PERICARDITIS SYNDROME MASQUARADING AS JUVUNILE IDIOPATHIC ARTHRITIS
Publikováno v:
Khyber Medical University Journal, Vol 10, Iss 4, Pp 221-223 (2018)
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is a rare autosomal recessive disease characterized by congenital or early-onset camptodactyly, childhood-onset non-inflammatory arthropathy associated with synovial hyperplasia, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e90ad482c13b38e278d50f29e8b4f37
http://www.kmuj.kmu.edu.pk/article/view/18072/pdf
http://www.kmuj.kmu.edu.pk/article/view/18072/pdf
Publikováno v:
International Journal of Medical Reviews and Case Reports, Vol 3, Iss 7 (2019)
Introduction: Pentalogy of Cantrell (PS) or Cantrell Sydrome (CS), first described by Cantrell in 1958, is a rare congenital anomaly characterized by defect in lower sternum, anterior abdominal wall defect, defect in anterior diaphragm, ectopia cordi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c23685cb453c40f7a1c7a056905c840
http://www.mdpub.net/index.php?fulltxt=44546
http://www.mdpub.net/index.php?fulltxt=44546