A. Akarsu

发表

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, Human molecular genetics.

From Allergen Molecules to Molecular Immunotherapy of Nut Allergy: A Hard Nut to Crack

R. Valenta, M. van Hage, M. Khaitov, 2021, Frontiers in Immunology.

Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.

M. Sarfarazi, N. Akarsu, M. Barsoum-Homsy, 1995, Genomics.

Food‐induced anaphylaxis in infants, as compared to toddlers and preschool children in Turkey

U. Sahiner, B. Sekerel, O. Soyer, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

M. Brodsky, B. Hart, J. Demer, 2003, Nature Genetics.

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).

P. Mullaney, J. Demer, D. Mackey, 2004, Investigative ophthalmology & visual science.

COVID-19 in Patients with Primary Immunodeficiency

I. Tezcan, D. Çağdaş, A. Akarsu, 2021, Journal of clinical immunology.

IgE mediated food allergy in Turkey: different spectrum, similar outcome.

B. Sekerel, Ö. Soyer, Ü. Şahiner, 2021, The Turkish journal of pediatrics.

Male cells in female recipients of hematopoietic-cell transplants.

A. Akarsu, A. Kaygusuz, A. Tuncer, 2002, The New England journal of medicine.

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.

M. Sarfarazi, A. Akarsu, B. Şayli, 1996, Human molecular genetics.

(synpolydactyly). 2 Homozygous phenotype?

M. Sarfarazi, U. Şaylı, O. Akhan, 2022 .

Hereditary intraosseous vascular malformation of the craniofacial region: an apparently novel disorder.

I. Vargel, B. Çil, Y. Erk, 2002, American journal of medical genetics.

Multiple synostosis type 2 (SYNS2) maps to 20q11.2 and caused by a missense mutation in the growth/differentiation factor 5 (GDF5).

T. Rezaie, M. Sarfarazi, D. Farhud, 1999 .

IgE-mediated food allergy throughout life

Ü. Şahiner, A. Akarsu, E. Celebioglu, 2020, Turkish journal of medical sciences.

Hypersensitivity Reactions to Biologicals: from Bench to Bedside

B. Sekerel, O. Soyer, A. Akarsu, 2020, Current Treatment Options in Allergy.

Food Allergy Management Has Been Negatively Impacted During the COVID-19 Pandemic

E. Aytekin, B. Sekerel, O. Soyer, 2021, Asthma Allergy Immunology.

Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.

A. Child, G. Brice, M. Sarfarazi, 1998, American journal of human genetics.

Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, American journal of medical genetics.

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.

M. Sarfarazi, N. Akarsu, U. Şaylı, 1995, Journal of medical genetics.

Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker.

M. Sarfarazi, A. Akarsu, B. Şayli, 1995, Human molecular genetics.

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21.

M. Sarfarazi, A. Akarsu, I. Stoilov, 1997, Human molecular genetics.

Oral food challenge in IgE mediated food allergy in eastern Mediterranean children.

B. Sekerel, Ö. Soyer, Ü. Şahiner, 2021, Allergologia et immunopathologia.

COVID-19 in Patients with Primary Immunodeficiency

I. Tezcan, D. Çağdaş, A. Akarsu, 2021, Journal of Clinical Immunology.

A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12.

E. Engle, A. Akarsu, E. C. Şener, 2000, Archives of ophthalmology.

BIGH3 Gene Analysis in the Differential Diagnosis of Corneal Dystrophies

S. Duman, A. Akarsu, A. Kocak-Altintas, 2001, Cornea.

DACH: genomic characterization, evaluation as a candidate for postaxial polydactyly type A2, and developmental expression pattern of the mouse homologue.

K Takahashi, H. Slavkin, T. Ikura, 2001, Genomics.

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

M. Sarfarazi, U. Şaylı, O. Akhan, 1995, Journal of medical genetics.

Co‐sensitization to the fruit seeds and raw potato in children with cashew nut allergy

E. Birben, U. Sahiner, B. Sekerel, 2020, Allergy.

Oral Immunotherapy in Food Allergy: A Critical Pediatric Perspective

A. Fiocchi, A. Zicari, S. Arasi, 2022, Frontiers in Pediatrics.

Exploring the Heterogeneity of IgE-Mediated Food Allergy through Latent Class Analysis

U. Sahiner, B. Sekerel, O. Soyer, 2022, International Archives of Allergy and Immunology.

Identification of KIF 21 A Mutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 ( CFEOM 3 )

P. Mullaney, J. Demer, D. Mackey, 2004 .

Is vitamin D hypothesis for schizophrenia valid? Independent segregation of psychosis in a family with vitamin-D-dependent rickets type IIA

T. Coşkun, A. Akarsu, H. Okur, 2004, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Food‐induced anaphylaxis in infants, as compared to toddlers and preschool children in Turkey

U. Sahiner, B. Sekerel, O. Soyer, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Cytogenetic and Phenotypic Findings in Turkish Patients With Fanconi's Anemia

A. Akarsu, Hatice Ilgin, Fatma Işik Bökesoy, 1999 .

Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population.

A. Bakkaloğlu, S. Ozen, M. Sarfarazi, 1997, Journal of medical genetics.

U. Sahiner, B. Sekerel, O. Soyer, 2021, Allergy and asthma proceedings.

Safety and efficacy of rapid drug desensitization in children

U. Sahiner, B. Sekerel, O. Soyer, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Phenotypic variability of triphalangeal thumb-polysyndactyly syndrome linked to chromosome 7q36.

S. Balcı, B. Civelek, A. Akarsu, 1999, American journal of medical genetics.

Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

E. Percin, I. Sezgin, S. Percin, 1998, Journal of medical genetics.

Multiplex component-based allergen macroarray test is useful to predict clinical reactivity to tree nuts in children.

U. Sahiner, B. Sekerel, O. Soyer, 2021, Allergology international : official journal of the Japanese Society of Allergology.

A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects

I. Tezcan, Ö. Sanal, D. Çağdaş, 2022, Scandinavian journal of immunology.

Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis.

A. Karaduman, M. Özgüç, A. Akarsu, 2017, The Turkish journal of pediatrics.

Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity.

H. Topaloglu, K. Gücüyener, A. Karaduman, 1998, Neuropediatrics.