Çocuk Nefrolojisi Bilim Dalı

Dr. Öğr. Üyesi Bahriye Atmış

 

1-PERSONAL PROFILE

      Name:  Bahriye                                                            Sex: Female

      Surname: ATMIŞ                                                      

     Adress:Cukurova University, Department of Pediatric Nephrology, Adana,TURKEY

      Date of Birth:  27/01/1985                                           E-mail: bahriyeatmis@gmail.com

2-EDUCATION and WORK EXPERIENCE

      Medical School: Cukurova University, Adana, TURKEY, 2002-2008

      Residency: Cukurova University, Pediatrics, Adana, Turkey, 2009-2013

      Fellowship: Cukurova University, Pediatric Nephrology, Adana, Turkey, 2014-2017

      Assistant Professor: Cukurova University,Pediatric Nephrology, Adana,Turkey,2019

      Other: Observer, Great Ormond Street Hospital, Pediatric Nephrology, London, UK, March-May 2016

3- PRESENT POSITION: Assitant Professor, Cukurova University, Faculty of Medicine, Department of Pediatric Nephrology

4-PRIZES and AWARDS

Young investigator award, 39th National Hematology Congress, 2013

5-JOURNAL PUBLICATIONS

       a)Publications  Indexed  By  Web  of  Science

1-     Atmis B, Turan İ, Melek E, Karabay Bayazit A. An infant with hyponatremia, hyperkalemia, and metabolic acidosis associated with urinary tract infection: Questions. Pediatr Nephrol. 2019 May 3. doi: 10.1007/s00467-019-04252-4. [Epub ahead of print]

2-     Atmis B, Turan İ, Melek E, Bayazit AK. An infant with hyponatremia, hyperkalemia, and metabolic acidosis associated with urinary tract infection: Answers. Pediatr Nephrol. 2019 May 3. doi: 10.1007/s00467-019-04254-2. [Epub ahead of print]

3-     Ekinci RMK, Balci S, Bisgin A, Atmis B, Dogruel D, Altintas DU, Yilmaz M. MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience. Postgrad Med. 2019 Jan;131(1):68-72. doi: 10.1080/00325481.2019.1552479.

4-     Atmis B, Bayazit A, Melek E, Bisgin A, Anarat A. Renal Features of Bardet Biedl Syndrome: A Single Center Experience. Turkish J ped  doi: 10.24953/turkjped.2019.002

5-     Atmış B, Kışla Ekinci RM, Melek E, Bisgin A, Yılmaz M, Anarat A, Bayazıt AK. Concomitance of familial Mediterranean fever and Gitelman syndrome in an adolescent. Turkish Jour Ped doi: 10.24953/turkjped.2019.001

6-     Kışla Ekinci RM, Balci S, Bisgin A, Atmis B, Dogruel D, Yılmaz M. Autoimmune Manifestations in Heterozygote Type I Complement 2  Deficiency: A Child Eventually Diagnosed With Systemic Lupus Erythematosus. Arch Rheumatol 2019;34(x):i-iv doi: 10.5606/ArchRheumatol.2019.6910

7-     Kisla Ekinci RM, Balci S, Bisgin A, Hershfield M, Atmis B, Dogruel D, Yilmaz M. Renal Amyloidosis in Deficiency of Adenosine Deaminase 2: Successful Experience With Canakinumab. Pediatrics. 2018 Nov;142(5). pii: e20180948. doi: 10.1542/peds.2018-0948.

8-     Bakkaloglu SA, Kandur Y, Serdaroğlu E, Noyan A, Bayazıt AK, Taşdemir M, Özlü SG, Özçelik G, Dursun İ, Alparslan C, Akcaboy M, Atikel YÖ, Parmaksız G, Atmış B, Sever L. Time-averaged hemoglobin values, not hemoglobin cycling, have an impact on outcomes in pediatric dialysis patients. Pediatr Nephrol. 2018 Nov;33(11):2143-2150. doi: 10.1007/s00467-018-4013-4.

9-     Alparslan C, Yavaşcan Ö, Kasap Demir B, Atmiş B, Karabay Bayazit A, Leblebisatan G, Öncel EP, Alaygut D, Mutlubaş F, Aksu N. Successful Management of a Rare Cause of Hemolytic Uremic Syndrome With Eculizumab in a Child. J Pediatr Hematol Oncol. 2018 Mar 23. doi: 10.1097/MPH.0000000000001121. [Epub ahead of print]PMID: 29578925

10-  Melek E, Bulut FD, Atmış B, Yılmaz BŞ, Bayazıt AK, Mungan NÖ. An ignored cause of red urine in children: rhabdomyolysis due to carnitine palmitoyl transferase II (CPT-II) deficiency. J Pediatr Endocrinol Metab. 2017 Feb 1;30(2):237-239. doi: 10.1515/jpem-2016-0324.PMID: 28085674

11-  Melek E, Aynacı S, Atmış B, Yöntem A, Uğuz A, Bayazıt AK. A rare manifestation of renal osteodystrophy in a non-compliant hemodialysis child: Questions. Pediatr Nephrol. 2016 Sep;31(9):1449-50. doi: 10.1007/s00467-015-3121-7. Epub 2015 May 13. No abstract available. PMID: 25966785

12-  Melek E, Aynacı S, Atmış B, Yöntem A, Uğuz A, Bayazıt AK. A rare manifestation of renal osteodystrophy in a non-compliant child on hemodialysis: Answers. Pediatr Nephrol. 2016 Sep;31(9):1451-3. doi: 10.1007/s00467-015-3124-4. Epub 2015 May 13. No abstract available. PMID: 25966786

 

       b) Publications  Indexed  By  other  than Web of Science

  1. Atmış B, Kılınç Y , Yılmaz M , Atmış A , Karagün B , Şaşmaz  H. T helper, cytotoxic T, and natural killer T cell profiles and their association with clinical prognosis in children with sickle cell anemia. Cukurova Medical Journal 2018; 43 (4): 1-1. DOI: 0.17826/cumj.408559 
  2. Atmış B, Bayazit AK, Melek E, Çağlı Ç, Anarat A. The incidence of Post-infectious glomerulonephritis: a single center results. Cukurova Med J 2018;43(Suppl 1):194-198 DOI: 10.17826/cumj.441742
  3. Atmış B, Melek E, Haliloğlu B, Karabay Bayazıt A, Anarat A.  Aquaporin 2 mutasyonu saptanan konjenital nefrojenik diabetes insipiduslu bir olgu. Cukurova Medical Journal,2018; 43 (4): 8-8. DOI: 10.17826/cumj.379198
  4. Melek E, Atmış B, Karabay Bayazıt A, Anarat A. Linezolid-induced thrombocytopenia in two patients with renal dysfunction. Cukurova Medical Journal 2016; 41 (4): 808-810. DOI: 10.17826/cutf.254552
  5. Melek E, Aynacı S, Atmış B, Erdem S , Özbarlas N , Bayazıt A . An ignored cause of chronic kidney disease in children: type 2 cardiorenal syndrome. Cukurova Medical Journal  2016; 41 (2): 393-395. DOI: 10.17826/cutf.206698

 

 

      c)National Publications

1.      Gemici A, Atmış B, Atmış A. "Kusma Ve Hipokalemi İle Başvuran Çocuk Olguda Bilateral Renal Arter Darlığı Bilateral Renal Artery Stenosis in Children With Vomiting and Hypokalemia". Bozok Tıp Dergisi 9 (2019): 172-176

2.      Duyuler Ayçin G, Atmış B , Şaşihüseyinoğlu A , Ufuk Altıntaş D , YılmazM . "Çocukta Antifosfolipid Sendromu: Olgu Sunumu Antiphospholipid Syndrome in Children: Case report". Bozok Tıp Dergisi 9 (2019): 169-171

3.      Gemici A, Atmış B, Ergün R . "Çocuklarda üriner sistem taşı klinik görünümü ve metabolik özellikleri: Tek merkez deneyimi". Acta Medica Alanya 3 (2019): 59-66

4.      Atmış B, Altıntaş D, Bayazıt AK, Leblebisatan G, Şaşmaz Hİ, Melek E, Kılınç Y, Anarat A. Fankoni Aplastik Anemili Çocuklarda Genitoüriner Sistem Anomalileri.  Türkiye Çocuk Hastalıkları dergisi [S.l.], jul. 2018. DOI: 10.12956/tjpd.2018.372

5.      Tolunay İ, Yıldızdaş RD, Horoz ÖÖ, Melek E, Atmış B, Yüksel B, Turan İ. Ev Tipi Ventilatör ile İzlenen Trakeostomili Hastalarda Ürolitiazis Sıklığı ve Risk Faktörleri. J Pediatr Emerg Intensive Care Med 2017;4:92-95. DOI: 10.4274/cayd.96158

6.      Atmış B, Orhan Ok Z, Melek E, Bayazıt AK, Anarat A. Erken Başlangıçlı Gitelman Sendromu olgusu.  Türkiye Çocuk Hastalıkları Dergisi [S.l.], jul. 2018. DOI: 10.12956/tjpd.2018.368 = 1 PUAN

7.      Burgaç E, Bulut FD, Şeker Yılmaz B, Atmış B, Önenli Mungan HS. Three Cases with Complete And Incomplete Lesch-Nyhan Syndrome and First Time Situs Inversus Totalis Unionity. Arch Pediatr 2017;2(1): 13-15 doi:10.5799/ahinjs.04.2017.02.008

8.      Atmış B, Bayazıt AK. Pediatrik Nefrolog Gözüyle Üriner Enfeksiyonlar. Turkiye Klinikleri J Urology-Special Topics 2015;8(4):50-5.

 

6-PRESENTATIONS:

      

 

a)Oral Presentations  on International Meetings

  1. Atmış B. Follow-up and treatment results of children with primary monosymptomatic nocturnal enuresis. 18Th international Eastern Mediterranean Family Medicine Congress, 2019
  2. Atmış B, Cevizli D, Şahin G, Melek E, Bayazıt AK. Çocuklarda Biyopsi Ile Gösterilmiş Akut Poststreptokoksik Glomerülonefritlerin Özellikleri. Uluslararası Katılımlı 10. Çocuk Nefroloji Kongresi S-28, 2019
  3. Ergün R, Şekerci ÇA, Atmış B, Gemici A, Tanıdır Y. Miyelodisplazili Çocuklarda Aynı Seansta Ardışık Yapılan Dolum Sistometrisinin Anlamı Var Mıdır? Uluslararası Katılımlı 10. Çocuk Nefroloji Kongresi S-23, 2019
  4. Mutlubaş F, Yel S, Soyaltın E, Kara A, Torun Bayram M, Tekcan D, Atmış B, Bakkaloğlu SA, Dursun İ, Gürgöze MK, Bayazit AK, Serdaroğlu E, Kenan B, Yılmaz A, Kavukç S, Bilge I, Kalyoncu M, Ekim M, Akil İ, Yüksel S, Kaplan Bulut İ, Anarat A, Tabel Y, Gökçe İ, Ertan P, Düşünsel R. Çocukluk Çağı İdiyopatik Nefrotik Sendromunda Mikofenolat-Mofetil Etkinliği. Uluslararası Katılımlı 10. Çocuk Nefroloji Kongresi S-29, 2019
  5. Ergün R, Şekerci ÇA, Tanıdır Y, Atmış B, Gemici A. Vezikoüreteral Reflünün İşeme Sistoüretrografisinde Dolum Ya Da İşeme Fazında Saptanmasının Üst Üriner Sistem Hasarı Üzerine Etkisi. S15. 10. Ulusal Pediatrik Üroloji Kongresi, 2019
  6. Alpay H, Tülpar S, Baştuğ F, Demircin G, Ağbaş A, Gemici A, Gökçe İ, Yürük Yıldırım Z, Gündüz Z, Çam Delebe Ö, Bulum B,  Atmış B, Sak M, Yılmaz K, Aksu B, Patat Öner N, Çelik B, Sürmeli Döven S, Ertan P, Çomak E, Özdemir Atikel Y, Karabağ Yılmaz E, Elmacı M. Mikrolitiaziste İlaç Başlamada Acele Etmeyelim: Çok Merkezli Bir Yıllık İzlem. Uluslararası Katılımlı 10. Çocuk Nefroloji Kongresi S-16, 2019
  7. Şeker Yılmaz B, Kor D, Bulut FD, Kılavuz S, Atmış B, Melek E, Bayazıt AK, Erdem E, Noyan A, Ceylaner S, Mungan NÖ. Yirmiyedi Sistinozis Hastasının Uzun Dönem Tedavi Sonuçları. VI. Uluslararası Katılımlı Lizozomal Hastalıklar Kongresi S07. 2018

 

       b)Oral Presentations  on  National Meetings

  1. Atmış B, Kılınç Y, Yılmaz M, Atmış A, Karagün BŞ, Şaşmaz İ. Orak Hücre Anemili Hastalarda İskemik Atakalarda T Helper, T Sitotoksik ve Natural Killer Hücre Profili ve Klinik Prognozla İlişkisi. 39. Ulusal Hematoloji Kongresi 2013; 91.
  2. Atmış B, Melek E, Aynacı S, Bayazıt AK. Çocukluk Çağı Nefrotik Sendromların Nadir Nedeni Olan C1q Nefropatili Bir Olgu. 3. PUADER Kongresi Sözel Bildiri 4. 2014; 62.
  3. Bayazıt AK, Atmış B, Kör D, Önenli Mungan N, Anarat A. Sistinozis ve herediter multiple ekzositoz birlikteliği. 8. Ulusal Çocuk Nefroloji Kongresi S-017. 2014.
  4. Atmış B, Bayazıt AK, Melek E, Anarat A. Bardet Biedl Sendromunda Renal Bulgular: Tek merkez deneyimi. S05, 2.Genç Pediatristler Kongresi, 2016
  5. Atmış B, Bayazıt AK, Melek E, Bişgin A, Anarat A. Çukurova Üniversitesi’nde Takip Edilen dRTA’lı Çocuk Hastaların Fenotipik ve Genotipik Özelliklerinin Değerlendirilmesi. 4.Olgu panayırı, Sözel Bildiri, 2017
  6. Atmış B, Gemici A, Güllü UU, Laloğlu F, Ergün R. Konjenital Böbrek ve üriner kanal anomalisi olan çocuklarda kardiyak anomaliler. 17. Çukurova Pediatri Günleri 21-22 Şubat 2019,Adana

 

       c)Poster Presentations on International Meetings

  1. Yüksekkaya İ, Karabay Bayazit A, Aynaci S, Atmis B, Anarat A. Ambulatory Blood Pressure Monitoring In Children With Unilateral Partial Ureteropelvic Junction Obstuction. The 47th ESPN Congress in Porto P65. Pediatric Nephrology 2014; 29: 1706.
  2. Melek E, Aynaci S, Atmis B, Yontem  A, Uguz A, Bayazit AK. Brown Tumor At The Maxillary Sinus: A Rare Manifestation Of Renal Osteodystrophy In A Non-compliant Hemodialysis Child. The 47th ESPN congress in Porto P277 Pediatric Nephrology 2014; 29: 1771.
  3. Melek E, Aynaci S, Atmis B, Erdem S, Özbarlas N, Bayazit AK. Type 2 Cardiorenal Sydrome In A Child: What The Nephrologist Needs To Know. The 47th ESPN congress in Porto P402. Pediatric Nephrology 2014; 29: 1808.
  4. Melek E, Anarat A, Atmış B, Bayazıt AK. Prevelance of dyskalemia in different pediatric patient groups. The 47th ESPN congress in Porto P479. Pediatric Nephrology 2014; 29: 1831.
  5. Atmış B, Melek E, Aynacı S, Narlı N, Bayazıt AK. Urinary ascites and perirenal urinoma in a newborn with trisomy 8 mosaicism. The 47th ESPN Congress in Porto P456. Pediatric Nephrology 2014; 29: 1824.
  6. Atmış B, Melek E, Bayazıt Y, Bayazıt AK, Anarat A. A Rare Cause of Anuric Acute Kidney Injury: Bilateral Ureterolithiasis. The 48th ESPN Congress in Brussels P13. Pediatric Nephrology 2015; 30: 1571.
  7. Aynaci S, Bayazıt AK,  Melek E, Gurbuz F, Atmis B, Anarat R, Yuksel B, Anarat A. Early Diabetic Nephropathy and Endothelial  Dysfunction in Children with Type1 Diabetes Mellitus. The 48th ESPN Congress in Brussels P212. Pediatric Nephrology 2015; 30: 1632.
  8. Melek E, Atmis B, Bayazit AK, Anarat A. Is There An Increased Risk Of Linezolid-Induced Thrombocytopenıa In Patients With Renal Dysfunction? Report Of Two Cases. The 48th ESPN Congress in Brussels P114. Pediatric Nephrology 2015; 30: 1600.
  9. Melek E, Atmış B, Aynacı S, Bayazıt AK, Anarat A. A Rare Cause of Systemic Hypertension in a Child: Liddle’s Syndrome. The 48th ESPN Congress in Brussels P284. Pediatric Nephrology 2015; 30: 1656.
  10. Melek E, Atmış B, Erdem S, Bayazıt AK, Anarat A. Nephrotic  Syndrome in a Patient with Kawasaki Disease. The 48th ESPN Congress in Brussels P400. Pediatric Nephrology 2015; 30: 1697.
  11. Atmış B, Melek E, Bayazıt AK, Yıldızdaş D, Aksungur E, Satar N, Erdoğan S, Anarat A. Malign hypertension due to angiodysplasia within the metanephric stromal tumor in an infant. 17th IPNA Congress, Iguaçu, Brazil PO623. Pediatric Nephrology 2016; 31: 1963.
  12. Atmis B, Bayazit AK, Melek E, Bisgin A, Anarat A. Clinical and genetic features of congenital nephrogenic diabetes insipidus: A Single Center Experience. 17th IPNA Congress, Iguaçu, Brazil PO138. Pediatr Nephrol 2016; 31:1809
  13. Atmis B, Bayazit AK, Melek E, Anarat A. Renal Features of Bardet Biedl Syndrome: A Single Center Experience. 17th IPNA Congress, Iguaçu, Brazil PO159  Pediatr Nephrol 2016;31:1815.
  14. Atmış B, Bayazıt AK,  Melek E, Cagli C , Anarat A. Is the Incidence of Postinfectious Glomerulonephritis Increasing?: Cases with Postinfectious Glomerulonephritis From a Single Center in November-December 2016. The 50th ESPN Congress in Glasgow P419. Pediatric Nephrology 2017; 32: 1751.
  15. Atmış B, Bayazıt AK,  Melek E, Yılmaz M , Bişgin A,  Anarat A. Attention to Chromosome 16: A Male Child With Association of SCL12A3 and M694V Homozygous Mutation. The 50th ESPN Congress in Glasgow P419. Pediatric Nephrology 2017; 32: 1816.
  16. Cagli C, Erdem S, Atmis B, Bayazit AK, Demir F, Demir H, Özbarlas N.  Renal Tract Anomalies in Children with Congenital Heart Disease Detected During the Procedure of Cardiac Catheterization. 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7-10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe, Bükreş, ROMANYA, 7-10 Haziran 2017, vol.102, no.2 P314. Arch Dis Child 2017; 102: A155. doi: 10.1136/archdischild-2017-313273.402
  17. Atmış B, Bayazıt AK,  Melek E, Sapmaz M, Demircan N,  Anarat A. Partial Whitening of Hair, Nistagmus and End Stage Renal Failure: Clues For Nephronophthisis Related Dısease. 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7-10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe, Bükreş, ROMANYA, 7-10 Haziran 2017, vol.102, no.2, pp.69-69. P92.  Arch Dis Child 2017; 102: A69. doi: 10.1136/archdischild-2017-313273.180
  18. Altintaş D, Atmiş B, Bayazit AK, Leblebisatan G, Şaşmaz HI, Melek EM, Anarat A, Kilinç A. Analysis of Genitourinary Anomalies In Patients with Fanconi Aplastic Anaemia. 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7-10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe, Bükreş, ROMANYA, 7-10 Haziran 2017, vol.102, no.2, pp.152-152. P308. Arch Dis Child 2017; 102: A152.
  19. Bayazıt AK, Atmış B, Melek E, Ala AS, Sapmaz M, Altunbaşak S,  Anarat A. An Uncommon Reason of End Stage Renal Disease: 3 Cases with Joubert Syndrome and Renal Failure. 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7?10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe, Bükreş, ROMANYA, 7-10 Haziran 2017, vol.102, no.2, pp.71-72. P97 Arch Dis Child 2017; 102: A71-A72. doi: 10.1136/archdischild-2017-313273.185
  20. Mungan NÖ, Bulut FD, Şeker-Yılmaz B, Kılavuz S, Kör D, Koç F, Gürkan E, Paydaş S, Güvenç B, Atmış B, Deniz A. Cukurova University experience of lysosomal diseases in adulthood: Report of 57 patients. 14th Annual WORLDSymposium  P254. Molecular Genetics and Metabolism 2018; 123: 100 https://doi.org/10.1016/j.ymgme.2017.12.263
  21. Atmis B, Bayazit AK,  Melek E, Bişgin A, Anarat A. Evaluation of phenotypic and genotypic features of distal renal tubular acidosis in children. 51st Annual ESPN Meeting, Antalya, P434Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  22. Sapmaz M, Sahin G, Turan I, Atmis B, Melek E, Bayazıt AK. Attention to transient pseudohypoaldosteronism in infancy with pyelonephritis. 51st Annual ESPN Meeting, Antalya, P414 Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  23. Atmis B, Atmis A, Yaralı O, Esmeray P, Gemici A. Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature. 51st Annual ESPN Meeting, Antalya, P294 Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  24. Ozcelik C, Anarat A, Mungan NO, Bisgin A,  Atmis B, Melek E, Bayazıt AK. Clinic and genetic presentation of children with cystinuria. 51st Annual ESPN Meeting, Antalya, P250 Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  25. Gorur O, Bayazıt AK, Atmis B, Melek E, Ozcelık C, Inal TC, Cetiner S, Anarat A. Early Determination of Renal Injury in Children with Solitary Functioning Kidney. 51st Annual ESPN Meeting, Antalya, P74 Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  26. Ozcan SC, Atmis B,  Melek E, Bayazıt AK. Risk factors of urinary tract infection in children performing clean intermittent catheterization. 51st Annual ESPN Meeting, Antalya, P56  Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  27. Gemici A, Atmış B, Ergün R, Kurnaz E, Yaralı O, Çayır A. A rare cause of secondary hypertension in a girl: 17 alpha hydroxylase deficiency. 51st Annual ESPN Meeting, Antalya, P217  Pediatr Nephrol (2018) 33: 1807-2008. https://doi.org/10.1007/s00467-018-4028-x
  28. Gemici A, Atmis B, Akay AC, Yaralı O, Çayır A. Late diagnosis of renal fanconi sydrome with HNF4A mutation in child with hypophospatemic rickets. 51st Annual ESPN Meeting, Antalya, P428 Pediatr Nephrol (2018) 33: 1807-2008.
  29. Atasever Yildirim G, Bulut FD, Atmiş B, Kilavuz S, Kör D, BayazitAK, Önenli Mungan NH. Fanconi bickel syndrome and renal tubular dysfunction GP287 9th Europaediatrics Dublin 2019, Archives of Disease in Childhood Jun 2019, 104 (Suppl 3) A151; DOI: 10.1136/archdischild-2019-epa.346
  30. Yıldırım SC, Şahin GS,  Atmış B, Turan İ, Melek E, Bayazıt AK. P561 Pseudohypoaldosteronism secondary to urinary tract infection in infants. 9th Europaediatrics Dublin 2019,Archives of Disease in Childhood Jun 2019, 104 (Suppl 3) A378; DOI: 10.1136/archdischild-2019-epa.895
  31. Atmış B, Cevizli D, Melek E, Bayazıt AK. İnfantlarda Üriner sistem taş hastalığı: tek merkez deneyimi. P029. Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  32. Atmış B, Cevizli D, Melek E, Bayazıt AK.  Son Dönem Kronik Böbrek Hastalığı Olan Çocuk Hastada Eksoftalmus ile Bulgu Veren Brown Tümörü P030. Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  33. Gemici A, Atmış B, Ergün R, Kurnaz E. Bilateral Hidronefrozlu Olguda Geç Konulan Tanı: Didmoad P084. Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  34. Baştuğ F, Alpay H, Gökçe İ, Gemici A, Dursun İ, Yürük Yıldırım Z, Bulum B, Atmış B, Sak M, Günay N, Demircin G, Tülpar S, Yılmaz K, Çam Delebe Ö, Elmacı M, Sürmeli Döven S, Çomak E, Çiçek N, Ağbaş A, Özdemir Atikel Y, Bakkaloğlu S, Ertan P, Çetinkaya H, Karabağ Yılmaz E. Çocuklarda Alt Pol Taşları: Çok Merkezli Bir Yıllık İzlem P091.  Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  35. Bakkaloğlu SA, Özdemir Atikel Y, Schmitt CP, Paglialonga F, Vondrak K, Yazıcıoğlu B, Jankauskiene A, Atmış B, Zurowska A..Avrupa Çocuk Nefroloji Merkezlerindeki Diyaliz Hastalarının Hastaneye Yatışı Üzerinde Etkili Faktörler: Epdwg/Espndwg Raporu   P093. Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  36. Cevizli D, Atmış B, Melek E, Bayazıt AK. 2017-2019 Yılları Arasında Periton Diyalizi Yapılan Hastalarda Peritonit Sıklığı   P137. Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019
  37. Gemici A, Atmış B, Ergün R. Çocuklarda Konjenital Böbrek Ve Üriner Kanal Anomalisi (CAKUT); Tek Merkez Deneyimi   P164.  Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, 2019

 

7-PROFESIONAL MEMBERSHIPS

Türk Nefroloji Derneği

Çocuk Nefroloji Derneği

European Society of Pediatric Nephrology

Türk Pediatri Kurumu

 

 

8-SCIENTEFIC PROJECTS

       a)International Scientefic Projects:

       b)National Scientefic Projects Supported by International Organizations:

9-EDITORIAL ACTIVITIES

10-CITATIONS ON WEB of SCIENCE

1-     Kisla Ekinci RM, Balci S, Bisgin A, Hershfield M, Atmis B, Dogruel D, Yilmaz M. Renal Amyloidosis in Deficiency of Adenosine Deaminase 2: Successful Experience With Canakinumab. Pediatrics. 2018 Nov;142(5). pii: e20180948. doi: 10.1542/peds.2018-0948.

a)      A Adrovic, O Kasapcopur. Pediatric rheumatology in Turkey. Rheumatology international, March 2019, Volume 39, Issue 3, pp 431–440

2-     Bakkaloglu SA, Kandur Y, Serdaroğlu E, Noyan A, Bayazıt AK, Taşdemir M, Özlü SG, Özçelik G, Dursun İ, Alparslan C, Akcaboy M, Atikel YÖ, Parmaksız G, Atmış B, Sever L. Time-averaged hemoglobin values, not hemoglobin cycling, have an impact on outcomes in pediatric dialysis patients. Pediatr Nephrol. 2018 Nov;33(11):2143-2150. doi: 10.1007/s00467-018-4013-4.

a)      U Querfeld, F Schaefer. Cardiovascular risk factors in children on dialysis: an update. Pediatric Nephrology, 2018 (2018). https://doi.org/10.1007/s00467-018-4125-x

b)     Lübbe, K., Nüsken, E., Rascher, K. et al. Glomerular disease patients have higher odds not to reach quality targets in chronic dialysis compared with CAKUT patients: analyses from a nationwide German paediatric dialysis registry. Pediatr Nephrol (2019) 34: 1229. https://doi.org/10.1007/s00467-019-04218