Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Anwar Qais Saadoon"'
Autor:
Khalil I. Al-Hamdi, MBChB, DDV, FICMS, FRCP, FAAD, MEADV, MMSSVD, Adel Gassab Mohammed, MD, CABMS, MSc, Ussama M. Makki, MBChB, FICMS (D & V), Dooha Khaleel Ismael, MBChB, CABMS (D & V), Anwar Qais Saadoon, MBChB
Publikováno v:
JAAD Case Reports, Vol 6, Iss 12, Pp 1345-1349 (2020)
Externí odkaz:
https://doaj.org/article/ba6d6133411c4ed984198148ac0c3899
Autor:
Alaa H. Al-Farhan, MBChB, FBMIS, Saad Abdulbaqi Alomar, MBChB, FIBMS (histopath.), DIU (Mol.cytogen.), Anwar Qais Saadoon, MBChB
Publikováno v:
JAAD Case Reports, Vol 6, Iss 4, Pp 381-382 (2020)
Externí odkaz:
https://doaj.org/article/585cbdc1e35c4e11af2a276f2f47a771
Autor:
Ussama M. Makki, Khalil I. Al-Hamdi, Adel Gassab Mohammed, Dooha Khaleel Ismael, Anwar Qais Saadoon
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 6, Iss 12, Pp 1345-1349 (2020)
JAAD Case Reports, Vol 6, Iss 12, Pp 1345-1349 (2020)
H syndrome is a rare autosomal recessive disorder that occurs because of mutations in the SLC29A3 gene, encoding the human equilibrative nucleoside transporter, which is a protein located in endosomes, lysosomes, and mitochondria.1, 2, 3, 4, 5 It was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a074cf662662b3b54b009ba81fb224d
http://europepmc.org/articles/PMC8064936
http://europepmc.org/articles/PMC8064936
Autor:
Anwar Qais Saadoon, Khalil I. Al-Hamdi
Publikováno v:
International Journal of Trichology
Acne conglobata (AC) is a rare form of severe and chronic nodulocystic acne. It is characterized by nodulocystic lesions, borrowing, interconnecting abscesses, scars, in addition to grouped comedones. AC usually appears on the trunk and may extend to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99a7d6922e039943de41f731049754bb
http://europepmc.org/articles/PMC7276160
http://europepmc.org/articles/PMC7276160
Publikováno v:
JAAD Case Reports
Dermatopathia pigmentosa reticularis (DPR) is an extremely rare autosomal dominant ectodermal dysplasia that occurs because of mutations in KRT14. It mainly affects the skin, nails, and hair, with a characteristic diagnostic triad of widespread retic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a012c4c66370d6eb2566ee347583747
https://doi.org/10.1016/j.jdcr.2019.02.014
https://doi.org/10.1016/j.jdcr.2019.02.014
Publikováno v:
JAMA dermatology. 156(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96cdc3016534f5be22ad5f9d17fe8359
https://pubmed.ncbi.nlm.nih.gov/32745176
https://pubmed.ncbi.nlm.nih.gov/32745176
Autor:
Anwar Qais Saadoon, Hakan Çelik
Publikováno v:
Cumhuriyet Medical Journal.
A 20-years-old female patient presented to the emergency service due to complaints of sudden onset of severe shortness of breath; by a 3-day history of fever and a 1-day history of dry cough. After the patient evaluation, the presence of SARS-COV-2 i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::226f41d743917a40dd1c4eddaeff71ba
https://doi.org/10.7197/cmj.vi.750276
https://doi.org/10.7197/cmj.vi.750276
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 6, Iss 4, Pp 381-382 (2020)
JAAD Case Reports, Vol 6, Iss 4, Pp 381-382 (2020)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b9e075cfb52adadc3d46e1faa21de9b
https://pubmed.ncbi.nlm.nih.gov/32337330
https://pubmed.ncbi.nlm.nih.gov/32337330
Publikováno v:
JAAD Case Reports
H syndrome is an autosomal recessive syndrome affecting multiple organ systems with a characteristic skin lesion. It occurs because of a mutation in the SLC29A3 gene.1 The first cases of this extremely rare syndrome were reported in consanguineous fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9693f9351e8661cf59764ce2b9a4b9f0
http://europepmc.org/articles/PMC6453830
http://europepmc.org/articles/PMC6453830
Autor:
Anwar Qais Saadoon
Publikováno v:
Essential Clinical Skills in Pediatrics ISBN: 9783319924250
The diagnosis of a patient’s problem is mainly based on careful history taking, so it is crucial to gather accurate information and data regarding the patient’s presenting complaint and further history, as much as possible. This chapter helps you
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9921d573e03a0af6b5557968e65a31c
https://doi.org/10.1007/978-3-319-92426-7_2
https://doi.org/10.1007/978-3-319-92426-7_2
