Search Results - "Nevin Yalman"

Squamous cell carcinoma development in Fanconi anemia patients who underwent hematopoietic stem cell transplantation by Anak, Sema, Yalman, Nevin, Bilgen, Hülya, Sepet, Elif, Deviren, Ayhan, Gürtekin, Başak, Tunca, Fatih, Başaran, Bora

“…We examined SCC development of 24 FA patients, who received HSCT from HLA‐matched relatives. In our BMT center, we applied low‐dose CY + LFI + ATG (n:13) as…”
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INVESTIGATION OF SALİVARY MIR-9 AND SERUM CIP2A LEVELS IN FANCONI ANEMIA PATIENTS AT HIGH RISK OF DEVELOPING ORAL SQUAMOUS CELL CARCINOMA by Zişan Asal Kılıç, Çetin Timur, Tülin Tiraje Celkan, Şahin Öğreden, Nevin Yalman

“…Objective: Fanconi anemia (FA) is a rare bone marrow failure syndrome caused by mutations in DNA repair genes, and the risk of developing Oral Squamous Cell…”
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INVESTIGATION OF SALIVARY miR-9, miR-34a ve miR-196a LEVELS IN FANCONI ANEMIA AND ORAL SQUAMOUS CELL CARCINOMA PATIENTS by Zisan Asal Kilic, Selcuk Dasdemir, Nevin Yalman, Tulin Tiraje Celkan, Bora Basaran, Haydar Murat Yener, Mehmet Güven Günver

“…Objective: Fanconi anemia (FA) is a rare bone marrow deficiency syndrome due to the DNA repair gene mutations, and Oral Squamous Cell Carcinoma (OSCC) is seen…”
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Two Possible Cases of Trichosporon Infections in Bone-Marrow-Transplanted Children: the First Case of T. japonicum Isolated from Clinical Specimens by Ağırbaşlı, Handan, Bilgen, Hulya, Özcan, Sema Keceli, Otlu, Baris, Sinik, Gulce, Çerikçioğlu, Nilgün, Durmaz, Riza, Can, Emine, Yalman, Nevin, Gedikoğlu, Gunduz, Sugita, Takashi

“…Trichosporon spp. are emerging as opportunistic agents that cause systemic diseases in immunocompromised hosts. Trichosporonosis carries a poor prognosis in…”
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Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis by ERICSON, Kim Göransdotter, FADEEL, Bengt, ANDERSSON, Mats, GUDMUNDSSON, Gudmundur H, GÜRGEY, Aytemiz, YALMAN, Nevin, JANKA, Gritta, NORDENSKJÖLD, Magnus, HENTER, Jan-Inge

“…Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disorder of immune regulation. Mutations in the gene encoding perforin were…”
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A Rare Presentation of 17α Hydroxylase/17,20 Lyase Deficiency in a Patient with non-Hodgkin's Lymphoma: A Case Report by Tekkeli, Niran, Kurt, Ilknur, Yalman, Nevin, Timur, Çetin, Demir, Şenol, Sağsak, Elif

“…17α‑hydroxylase/17,20‑lyase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia that causes decreased cortisol and sex steroid levels and leads…”
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Reactivation: A severe problem in familial hemophagocytic lymphohistiocytosis by Devecioglu, Omer, Yalman, Nevin, Biner, Betul, Anak, Sema, Agaoglu, Leyla, Unuvar, Aysegul, Sarper, Nazan, Gedikoglu, Gunduz

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Rab27a by Bahadoran, Philippe, Aberdam, Edith, Mantoux, Frédéric, Buscà, Roser, Bille, Karine, Yalman, Nevin, de Saint-Basile, Geneviève, Casaroli-Marano, Ricardo, Ortonne, Jean-Paul, Ballotti, Robert

“…Normal pigmentation depends on the uniform distribution of melanin-containing vesicles, the melanosomes, in the epidermis. Griscelli syndrome (GS) is a rare…”
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Characterization of PRF1, STX11 and UNC13D genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis by Horne, AnnaCarin, Ramme, Kim Göransdotter, Rudd, Eva, Zheng, Chengyun, Wali, Yasser, Al‐Lamki, Zakia, Gürgey, Aytemiz, Yalman, Nevin, Nordenskjöld, Magnus, Henter, Jan‐Inge

“…Summary Familial hemophagocytic lymphohistiocytosis (FHL) is a rare autosomal recessive lethal condition characterized by fever, cytopenia, hepatosplenomegaly…”
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Rab27a: A Key to Melanosome Transport in Human Melanocytes by Bahadoran, Philippe, Aberdam, Edith, Mantoux, Frédéric, Buscà, Roser, Bille, Karine, Yalman, Nevin, de Saint-Basile, Geneviève, Casaroli-Marano, Ricardo, Ortonne, Jean-Paul, Ballotti, Robert

“…Normal pigmentation depends on the uniform distribution of melanin-containing vesicles, the melanosomes, in the epidermis. Griscelli syndrome (GS) is a rare…”
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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis by Göransdotter Ericson, Kim, Fadeel, Bengt, Nilsson-Ardnor, Sofie, Söderhäll, Cilla, Samuelsson, AnnaCarin, Janka, Gritta, Schneider, Marion, Gürgey, Aytemiz, Yalman, Nevin, Révész, Tom, Egeler, R. Maarten, Jahnukainen, Kirsi, Storm-Mathiesen, Ingebjörg, Haraldsson, Ásgeir, Poole, Janet, de Saint Basile, Geneviève, Nordenskjöld, Magnus, Henter, Jan-Inge

“…Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of early childhood characterized by nonmalignant accumulation and…”
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G‐CSF‐mobilized haploidentical peripheral blood stem cell transplantation in children with poor prognostic nonmalignant disorders by Arpacı, Fikret, Tezcan, İlhan, Kuzhan, Okan, Yalman, Nevin, Uçkan, Duygu, Kürekçi, Ahmet Emin, İkincioğulları, Aydan, Özet, Ahmet, Tanyeli, Atilla

“…Haploidentical hematopoietic stem cell transplantation (HSCT) is currently one of the alternative curative treatment options for some nonmalignant but also for…”
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HLA-DRB115 and pediatric aplastic anemia by Oguz, FS, Yalman, N, Diler, AS, Oguz, R, Anak, S, Dorak, MT

“…We report a positive association between HLA-DRB1*15 (p= 0.0002) in Turkish patients with pediatric severe aplastic anemia (SAA) and a paradoxically favorable…”
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A male-specific increase in the HLA-DRB4 (DR53) frequency in high-risk and relapsed childhood ALL by Dorak, M.Tevfik, Oguz, Fatma S., Yalman, Nevin, Diler, A.Sarper, Kalayoglu, Sevgi, Anak, Sema, Sargin, Deniz, Carin, Mahmut

“…Previous studies reported significant HLA-DR associations with various leukemias one of which is with HLA-DRB4 (DR53) family in male patients with childhood…”
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Two Genes Are Responsible for Griscelli Syndrome at the Same 15q21 Locus by Pastural, Elodie, Ersoy, Fügen, Yalman, Nevin, Wulffraat, Nico, Grillo, Eugênio, Ozkinay, Ferda, Tezcan, Ilhan, Gediköglu, G., Philippe, Noël, Fischer, Alain, de Saint Basile, Geneviève

“…Griscelli syndrome is a rare autosomal recessive disease characterized by pigment dilution, variable cellular immunodeficiency, and an acute phase of…”
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The effect of bone marrow transplantation on systemic and oral health in Fanconi's aplastic anemia by Yalman, N, Sepet, E, Aren, G, Mete, Z, Külekçi, G, Anak, S

“…Fanconi's anemia (FA) is an autosomal-recessive disorder characterized by a progressive pancytopenia, diverse congenital abnormalities and increased…”
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HEPATIC ABNORMALITIES IN THALASEMIA MAJOR 83 by Anak, Sema, Emin, Dilek, Sarper, Nazan, Yalman, Nevin, Devecioglu, Ömer, Agaoglu, Leyla, Gedikoglu, Gündüz

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Fludarabine, cytarabine, G-CSF and idarubicin (FLAG-IDA) for the treatment of relapsed or poor risk childhood acute leukemia by Yalman, N, Sarper, N, Devecioğlu, O, Anak, S, Eryilmaz, E, Can, M, Yenilmez, H, Ağaoğlu, L, Gedikoğlu, G

“…The prognosis of relapsed acute leukemia or chronic leukemia in acute blast crisis is poor and new chemotherapeutic regimens could be useful for these…”
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Letter to the Editor:FLAG (fludarabine, high-dose cytarabine and G-CSF) for refractory and high-risk relapsed acute leukemia in children by Sarper, Nazan, Yalman, Nevin

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wt1 gene expression in childhood acute leukemias by Ozgen, U, Anak, S, Ozbek, U, Sarper, N, Eryilmaz, E, Ağaoğlu, L, Devecioğlu, O, Yalman, N, Gedikoğlu, G

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