Published: 2020-12-01

Plasmapheresis in a child with cold antibody autoimmune hemolytic anemia: case report

Zeynep Canan Özdemir, Özcan Bör, Ener Çağrı Dinleyici, Eylem Kıral

(169-172)

Gorlin-Goltz syndrome

Betül Şereflican, Bengü Tuman, Murat Şereflican, Sıddıka Halıcıoğlu, Gülzade Özyalvaçlı, Seval Bayrak

(173-177)

A congenital cranial dysinnervation disorder: Möbius’ syndrome

Hatice Mutlu Albayrak, Nuriye Tarakçı, Hüseyin Altunhan, Rahmi Örs, Hüseyin Çaksen

(165-168)

Hyperbilirubinemia due to minor blood group (anti-E) incompatibility in a newborn: a case report

Murat Özcan, Selin Sevinç, Vildan Boz Erkan, Yüksel Yurdugül, S. Ümit Sarıcı

(162-164)

When the Turkish word exists

Aves Editorial Aves Editorial

(186-186)

Erratum

Aves Editorial Aves Editorial

(185-185)

Evaluation of Candida species and antifungal susceptibilities among children with invasive candidiasis

Murat Sütçü, Manolya Acar, Gonca Erköse Genç, İlknur Kökçü, Hacer Aktürk, Gürkan Atay, Selda Hançerli Törun, Nuran Salman, Zayre Erturan, Ayper Somer

(145-153)

Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies

Ezgi Ulusoy Severcan, Neslihan Edeer Karaca, Güzide Aksu, Cengiz Çavuşoğlu, Necil Kütükçüler

(138-144)

Research of genetic bases of hereditary non-syndromic hearing loss

Aslı Subaşıoğlu, Duygu Duman, Aslı Sırmacı, Güney Bademci, Fehime Carkıt, Mehmet Akif Somdaş, Mustafa Erkan, Mustafa Tekin, Munis Dündar

(122-132)

Re: HLA genes as a predictive screening tool for celiac disease

Hale Tuhan, Sakine Işık, Ayhan Abacı, Erdem Şimsek, Ahmet Anık, Özden Anal, Ece Böber

(184-184)

HLA genes as a predictive screening tool for celiac disease

Hakim Rahmoune, Nada Boutrid, Mounira Amrane, Belkacem Bioud

(182-184)

Erroneous diagnosis of rickets

Stepan Kutilek, Sylva Skalova

(178-179)

Role of genetics in pediatric rheumatology

Eda Tahir Turanlı, Elif Everest, Ayşe Balamir, Aslı Kireçtepe Aydın, Özgür Kasapçopur

(113-121)