Kaymakcalan, Hande: search on Z-Library

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1

NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy

Caglayan, Ahmet Okay, Comu, Sinan, Baranoski, Jacob F., Parman, Yesim, Kaymakçalan, Hande, Akgumus, Gozde Tugce, Caglar, Caner, Dolen, Duygu, Erson-Omay, Emine Zeynep, Harmanci, Akdes Serin, Mishra-Go

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 1.14 MB

english, 2015

2

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature

Michael R. Rossi, Miriam S. DiMaio, Bixia Xiang, Kangmo Lu, Hande Kaymakcalan, Margretta Seashore, Maurice J. Mahoney, Peining Li

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 239 KB

english, 2009

3

Prenatal Health, Educational Attainment, and Intergenerational Inequality: The Northern Finland Birth Cohort 1966 Study

Juho Härkönen, Hande Kaymakçalan, Pirjo Mäki, Anja Taanila

Journal:

Year:

2012

Language:

english

File:

PDF, 311 KB

english, 2012

4

Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities

Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar,

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 991 KB

english, 2013

5

4861780 4(3H)-quinazolinone derivatives and pharmaceutical compositions

Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar,

Journal:

General Pharmacology: The Vascular System

Year:

1990

Language:

english

File:

PDF, 160 KB

english, 1990

6

In England Now

Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar,

Journal:

Year:

1988

Language:

english

File:

PDF, 158 KB

english, 1988

7

" WATCH WHAT YOU EAT"

Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar,

Journal:

Year:

1966

Language:

english

File:

PDF, 169 KB

english, 1966

8

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Schaffer, Ashleigh E., Breuss, Martin W., Caglayan, Ahmet Okay, Al-Sanaa, Nouriya, Al-Abdulwahed, Hind Y., Kaymakçalan, Hande, Yılmaz, Cahide, Zaki, Maha S., Rosti, Rasim O., Copeland, Brett, Baek, Se

Journal:

Nature Genetics

Year:

2018

Language:

english

File:

PDF, 3.38 MB

english, 2018

9

ALPK3 GENE MUTATION IN A PATIENT WITH CONGENITAL CARDIOMYOPATHY AND DYSMORPHIC FEATURES

Cağlayan, Ahmet Okay, Sezer, Rabia Gonul, Kaymakcalan, Hande, Ulgen, Ege, Yavuz, Taner, Baranoski, Jacob F., Bozaykut, Abdulkadir, Serin Harmanci, Akdes, Yalcin, Yalim, Youngblood, Mark W., Yasuno, Ka

Journal:

Molecular Case Studies

Year:

2017

Language:

english

File:

PDF, 379 KB

english, 2017

10

1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems

Kaymakçalan, Hande, Li, Peining

Journal:

Indian Journal of Pediatrics

Year:

2019

Language:

english

File:

PDF, 145 KB

english, 2019

11

Prenatal Health, Educational Attainment, and Intergenerational Inequality: The Northern Finland Birth Cohort 1966 Study

Juho Härkönen, Hande Kaymakçalan, Pirjo Mäki and Anja Taanila

Journal:

Year:

2012

Language:

english

File:

PDF, 2.56 MB

english, 2012

12

Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis

Marukian, Nareh V., Hu, Rong-Hua, Craiglow, Brittany G., Milstone, Leonard M., Zhou, Jing, Theos, Amy, Kaymakcalan, Hande, Akkaya, Deniz A., Uitto, Jouni J., Vahidnezhad, Hassan, Youssefian, Leila, Ba

Journal:

JAMA Dermatology

Year:

2017

Language:

english

File:

PDF, 853 KB

english, 2017

13

Novel compound heterozygous mutations in GPT2 linked to microcephaly, and intellectual developmental disability with or without spastic paraplegia

Kaymakcalan, Hande, Yarman, Yanki, Goc, Nukte, Toy, Fatih, Meral, Cihan, Ercan-Sencicek, A. Gulhan, Gunel, Murat

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 986 KB

english, 2017

14

Changes in peanut allergy prevalence in different ethnic groups in 2 time periods

Fox, Adam T., Kaymakcalan, Hande, Perkin, Michael, du Toit, George, Lack, Gideon

Journal:

Journal of Allergy and Clinical Immunology

Year:

2015

Language:

english

File:

PDF, 340 KB

english, 2015

15

Brain Malformations Associated With Knobloch Syndrome—Review of Literature, Expanding Clinical Spectrum, and Identification of Novel Mutations

Caglayan, Ahmet Okay, Baranoski, Jacob F., Aktar, Fesih, Han, Wengi, Tuysuz, Beyhan, Guzel, Aslan, Guclu, Bulent, Kaymakcalan, Hande, Aktekin, Berrin, Akgumus, Gozde Tugce, Murray, Phillip B., Erson-O

Journal:

Pediatric Neurology

Year:

2014

Language:

english

File:

PDF, 3.09 MB

english, 2014

16

[IEEE 2018 3rd International Conference on Computer Science and Engineering (UBMK) - Sarajevo, Bosnia and Herzegovina (2018.9.20-2018.9.23)] 2018 3rd International Conference on Computer Science and Engineering (UBMK) - The relationship between PAPP-A levels, maternal characteristics, gestational diabetes and other biochemical markers of the aneuploidy screening

Uzut, Ommu Gulsum, Celebiler, Hande Kaymakcalan, Harkonen, Juho, Bakir-Gungor, Burcu

Year:

2018

File:

PDF, 7 KB

2018

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