Publications by authors named "Serap Emre"

Claim this Profile
S
Splenic Gaucheroma Leading to Incidental Diagnosis of Gaucher Disease in a 46-Year-Old Man with a Rare GBA Mutation: A Case Report.
İzzet Erdal, Yılmaz Yıldız, Gizem Önal, Oktay Halit Aktepe, Selin Ardalı Düzgün, Serap Dökmeci Emre

Endocr Metab Immune Disord Drug Targets· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Application of Fourier transform infrared spectroscopy to biomolecular profiling of cultured fibroblast cells from Gaucher disease patients: A preliminary investigation.
Nasit Igci, Parisa Sharafi, Duygu Ozel Demiralp, Cemil Ozerk Demiralp, Aysel Yuce, Serap Dokmeci Emre

Adv Clin Exp Med· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation.
Banu Guzel Nur, Pinar Gencpinar, Ayse Yuzbasıoglu, Serap Dokmeci Emre, Ercan Mihci

Eur J Med Genet· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Outcome of enzyme replacement therapy in Turkish patients with Gaucher disease: does late intervention affect the response?
Zeynep Arikan-Ayyildiz, Aysel Yüce, Serap Emre, Gökhan Baysoy, Inci Nur Saltik-Temizel

Turk J Pediatr· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene.
Serap Emre, Neşe Unver, Sibel Ersoy Evans, Ayşe Yüzbaşioğlu, Figen Gürakan

Eur J Med Genet· October 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular analysis of Turkish Gaucher disease patients: identification of novel mutations in glucocerebrosidase (GBA) gene.
Serap Emre, Figen Gürakan, Aysel Yüce, Arnold Rolf, Ronald Scott

Eur J Med Genet· October 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multiple endocrine neoplasia type 2b associated with lichen nitidus.
Asli Altaykan, Sibel Ersoy-Evans, Serap Emre, Diclehan Orhan, Safak Güçer

Eur J Dermatol· November 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.
Fabienne Lesueur, Bakar Bouadjar, Caroline Lefèvre, Florence Jobard, Stéphanie Audebert, Serap Emre

J Invest Dermatol· April 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular analysis of Turkish mucopolysaccharidosis IVA (Morquio A) patients: identification of novel mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene.
Mugen Terzioglu, Aysegul Tokatli, Turgay Coskun, Serap Emre

Hum Mutat· December 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biochemical and molecular analysis of mucopolysaccharidoses in Turkey.
Serap Emre, Mügen Terzioğlu, Turgay Coşkun, Ayşegül Tokath, Imran Ozalp

Turk J Pediatr· March 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B.
Serap Emre, Mugen Terzioglu, Aysegul Tokatli, Turgay Coskun, Imran Ozalp

Hum Mutat· February 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.
Florence Jobard, Caroline Lefèvre, Aysen Karaduman, Claudine Blanchet-Bardon, Serap Emre

Hum Mol Genet· January 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis