• Glucocorticoid-Associated Worsening In Reversible Cerebral Vasoconstriction Syndrome 

      Singhal, Aneesh B.; Topcuoglu, Mehmet A. (Lippincott Williams & Wilkins, 2017)
      Objective: Factors predicting poor outcome in patients with the reversible cerebral vasoconstriction syndrome (RCVS) have not been identified. Methods: In this single-center retrospective study, we analyzed the clinical, ...
    • Glucose Intolerance, Insulin Resistance, And Hyperandrogenemia In First Degree Relatives Of Women With Polycystic Ovary Syndrome 

      Yildiz, BO; Yarali, H; Oguz, H; Bayraktar, M (Endocrine Soc, 2003)
      Polycystic ovary syndrome (PCOS) is associated with hyperinsulinemia, insulin resistance (IR), increased risk of glucose intolerance, and type 2 diabetes. Family studies have indicated a genetic susceptibility to PCOS. The ...
    • Glue Septal Ablation: A Promising Alternative To Alcohol Septal Ablation 

      Okutucu, Sercan; Aytemir, Kudret; Oto, Ali (2016)
      Hypertrophic cardiomyopathy (HCM) is defined as myocardial hypertrophy in the absence of another cardiac or systemic disease capable of producing the magnitude of present hypertrophy. In about 70% of patients with HCM, ...
    • Glutaric Aciduria Type 2 Presenting With Acute Respiratory Failure In An Adult 

      Ersoy, Ebru Ortac; Rama, Dorina; Ünal, Özlem; Sivri, Serap; Topeli, Arzu (2015)
      Glutaric aciduria (GTA) type II can be seen as late onset form with myopathic phenotype. We present a case of a 19-year old female with progressive muscle weakness was admitted in intensive care unit (ICU) with respiratory ...
    • Gluteal Calcinosis In A Patient With Undifferentiated Connective Tissue Disease: A Bulky Lesion Resected Surgically 

      Isik, Metin; Guner, Gunes; Yesilkaya, Yakup; Calguneri, Meral (Baycinar Medical Publ-Baycinar Tibbi Yayincilik, 2011)
      Calcinosis frequently accompanies rheumatologic diseases and mostly occurs after trauma, due to structural damage, hypovascularity, and tissue hypoxia. Calcinosis may be seen in a localized area or it may be widespread, ...
    • Gnrh Stimulation Test In Precocious Puberty: Single Sample Is Adequate For Diagnosis And Dose Adjustment 

      Kandemir, Nurgün; Demirbilek, Hüseyin; Özön, Zeynep Alev; Gönç, Nazlı; Alikaşifoğlu, Ayfer (2011)
      Objective: Gonadotropin stimulation test is the gold standard to document precocious puberty. However, the test is costly, time-consuming and uncomfortable. The aim of this study was to simplify the intravenous ...
    • Grace And The Development Of An Education And Training Curriculum 

      Finch, R. G.; Blasi, F. B.; Verheij, T. J. M.; Goossens, H.; Coenen, S.; Loens, K.; Rohde, G.; Saenz, H.; Akova, M. (Wiley-Blackwell, 2012)
      Clin Microbiol Infect 2012; 18: E308E313 Abstract Antimicrobial resistance is a serious threat and compromises the management of infectious disease. This has particular significance in relation to infections of the respiratory ...
    • Gray Platelet Syndrome: Natural History Of A Large Patient Cohort And Locus Assignment To Chromosome 3P 

      Gunay-Aygun, Meral; Zivony-Elboum, Yifat; Gumruk, Fatma; Geiger, Dan; Cetin, Mualla; Khayat, Morad; Kleta, Robert; Kfir, Nehama; Anikster, Yair; Chezar, Judith; Arcos-Burgos, Mauricio; Shalata, Adel; Stanescu, Horia; Manaster, Joseph; Arat, Mutlu; Edwards, Hailey; Freiberg, Andrew S.; Hart, P. Suzanne; Riney, Lauren C.; Patzel, Katherine; Tanpaiboon, Pranoot; Markello, Tom; Huizing, Marjan; Maric, Irina; Horne, McDonald; Kehrel, Beate E.; Jurk, Kerstin; Hansen, Nancy F.; Cherukuri, Praveen F.; Jones, Marypat; Cruz, Pedro; Mullikin, Jim C.; Nurden, Alan; White, James G.; Gahl, William A.; Falik-Zaccai, Tzippora (Amer Soc Hematology, 2010)
      Gray platelet syndrome (GPS) is an inherited bleeding disorder characterized by macrothrombocytopenia and absence of platelet alpha-granules resulting in typical gray platelets on peripheral smears. GPS is associated with ...
    • Griscelli Syndrome Restricted To Hypopigmentation Results From A Melanophilin Defect (Gs3) Or A Myo5A F-Exon Deletion (Gs1) 

      Menasche, G; Ho, CH; Sanal, O; Feldmann, J; Tezcan, I; Ersoy, F; Houdusse, A; Fischer, A; de Saint Basile, G (Amer Soc Clinical Investigation Inc, 2003)
      Griscelli syndrome (GS) is a rare autosomal recessive disorder that associates hypopigmentation, characterized by a silver-gray sheen of the hair and the presence of large clusters of pigment in the hair shaft, and the ...
    • Gross Deletions Involving Ighm, Btk, Or Artemis: A Model For Genomic Lesions Mediated By Transposable Elements 

      van Zelm, Menno C.; Geertsema, Corinne; Nieuwenhuis, Nicole; de Ridder, Dick; Conley, Mary Ellen; Schiff, Claudine; Tezcan, Ilhan; Bernatowska, Ewa; Hartwig, Nico G.; Sanders, Elisabeth A. M.; Litzman, Jiri; Kondratenko, Irina; van Dongen, Jacques J. M.; van der Burg, Mirjarn (Cell Press, 2008)
      Most genetic disruptions underlying human disease are microlesions, whereas gross lesions are rare with gross deletions being most frequently found (6%). Similar observations have been made in primary immunodeficiency ...
    • Growth Hormone Deficiency In A Child With Neurofibromatosis-Noonan Syndrome 

      Vurallı, Doğuş; Gönç, Nazlı; Vidaud, Dominique; Özön, Alev; Alikaşifoğlu, Ayfer; Kandemir, Nurgün (2016)
      Neurofibromatosis-Noonan syndrome (NFNS) is a distinct entity which shows the features of both NF1 (neurofibromatosis 1) and Noonan syndrome (NS). While growth hormone deficiency (GHD) has been relatively frequently ...
    • Growth Hormone Deficiency In The Transition Period 

      Vuralli, Dogus (2019)
      The importance of continuing growth hormone therapy in the transition and adulthood periods must be studied in adolescents with growth hormone deficiency with childhood onset. Continuation of growth hormone therapy during ...
    • Guanidinoacetate Methyltransferase (Gamt) Deficiency: Outcomes In 48 Individuals And Recommendations For Diagnosis, Treatment And Monitoring 

      Stockler-Ipsiroglu, Sylvia; van Karnebeek, Clara; Longo, Nicola; Korenke, G. Christoph; Mercimek-Mahmutoglu, Saadet; Marquart, Iris; Barshop, Bruce; Grolik, Christiane; Schlune, Andrea; Angle, Brad; Araujo, Helena Caldeira; Coskun, Turgay; Diogo, Luisa; Geraghty, Michael; Haliloglu, Goknur; Konstantopoulou, Vassiliki; Leuzzi, Vincenzo; Levtova, Alina; MacKenzie, Jennifer; Maranda, Bruno; Mhanni, Aizeddin A.; Mitchell, Grant; Morris, Andrew; Newlove, Theresa; Renaud, Deborah; Scaglia, Fernando; Valayannopoulos, Vassili; van Spronsen, Francjan J.; Verbruggen, Krijn T.; Yuskiv, Nataliya; Nyhan, William; Schulze, Andreas (Academic Press Inc Elsevier Science, 2014)
      We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) deficiency. Global developmental delay/intellectual disability (DD/ID) with speech/language delay and behavioral problems as ...
    • Guidance Document For Structured Reporting Of Diuresis Renography 

      Taylor, Andrew T.; Blaufox, M. Donald; De Palma, Diego; Dubovsky, Eva V.; Erbas, Belkis; Eskild-Jensen, Anni; Frokiaer, Jorgen; Issa, Muta M.; Piepsz, Amy; Prigent, Alain (W B Saunders Co-Elsevier Inc, 2012)
      This Guidance Document for structured reporting of diuresis renography in adults was developed by the International Scientific Committee of Radionuclides in Nephro-urology (ISCORN; http://www.iscorn.org). ISCORN chose ...
    • Guideline for PET/CT imaging of neuroendocrine neoplasms with 68Ga-DOTA-conjugated somatostatin receptor targeting peptides and 18F–DOPA 

      Bozkurt, Murat Fani; Virgolini, Irene; Balogova, Sona; Beheshti, Mohsen; Rubello, Domenico; Decristoforo, Clemens; Ambrosini, Valentina; Kjaer, Andreas; Delgado-Bolton, Roberto; Kunikowska, Jolanta; Oyen, Wim J. G.; Chiti, Arturo; Giammarile, Francesco; Fanti, Stefano (Springer, 2017)
      Purpose & Methods Neuroendocrine neoplasms are a heterogenous group of tumours, for which nuclear medicine plays an important role in the diagnostic work-up as well as in the targeted therapeutic options. This guideline ...
    • Guideline Implementation In A Multicenter Study With An Estimated 44% Relative Cardiovascular Event Risk Reduction 

      Onat, A; Soydan, I; Tokgozoglu, L; Sansoy, V; Koylan, N; Domanic, N; Ural, D (Clinical Cardiology Publ Co, 2003)
      Background: The extent of cardiovascular risk reduction by implementing coronary prevention guidelines needs to be documented in various population samples. Hypothesis: This is a multicenter study to assess the impact of ...
    • Guidelines For The Genetic Diagnosis Of Hereditary Recurrent Fevers 

      Shinar, Y; Obici, L; Aksentijevich, I; Bennetts, B; Austrup, F; Ceccherini, I; Costa, J M; De Leener, A; Gattorno, M; Kania, U; Kone-Paut, I; Lezer, S; Livneh, A; Moix, I; Nishikomori, R; Ozen, Seza; Phylactou, L; Risom, L; Rowczenio, D; Sarkisian, T; van Gijn, M E; Witsch-Baumgartner, M; Morris, M; Hoffman, H M; Touitou, I (2012)
      Hereditary recurrent fevers (HRFs) are a group of monogenic autoinflammatory diseases characterised by recurrent bouts of fever and serosal inflammation that are caused by pathogenic variants in genes important for the ...
    • Güncel Kılavuzlar Işığında Pulmoner Hipertansiyonda Tedavi Algoritmaları 

      Okutucu, Sercan; Tokgozoglu, Lale (Turkish Soc Cardiology, 2010)
      Pulmonary arterial hypertension (PAH) is a clinical syndrome that is often diagnosed late and is associated with a progressive clinical deterioration and death. However, over the past ten years there has been a dramatic ...
    • Güncellenmiş Türkiye Psoriasis Biyolojik Ajan Kullanım Kılavuzu 

      Alper, Sibel; Atakan, Nilguen; Gurer, Mehmet Ali; Onsun, Nahide; Ozarmagan, Guzin (Turkish Soc Dermatology Venerology, 2010)