عناروين إضافية: New hereditary polyposis syndromes in the patient with intestinal polyps

المصدر: Jelsig , A M , Jespersen , N , Karstensen , J G , Ketabi , Z , Rønlund , K , Sunde , L , Thorlacius-Ussing , O , Wadt , K , Qvist , N & Lautrup , C K 2021 , ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ' , Ugeskrift for Laeger , bind 183 , nr. 38 , :V02210148 . <

مصطلحات الفهرس: Colorectal Neoplasms, Genetic Testing, Humans, Intestinal Polyposis/diagnosis, Intestinal Polyps, Nasopharyngeal Neoplasms, Neoplastic Syndromes, Hereditary/diagnosis, article

URL: https://curis.ku.dk/portal/da/publications/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypperTest(e406d31e-3055-44bc-887a-bd4d5d0d9cee).html
https://curis.ku.dk/ws/files/337983106/v02210148_web.pdfTest
https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2022-03/v02210148_web.pdfTest

عناروين إضافية: New hereditary polyposis syndromes in the patient with intestinal polyps

المصدر: Jelsig , A M , Jespersen , N , Karstensen , J G , Ketabi , Z , Rønlund , K , Sunde , L , Thorlacius-Ussing , O , Wadt , K , Qvist , N & Lautrup , C K 2021 , ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ' , Ugeskrift for Laeger , bind 183 , nr. 38 , :V02210148 . <

مصطلحات الفهرس: Colorectal Neoplasms, Genetic Testing, Humans, Intestinal Polyposis/diagnosis, Intestinal Polyps, Nasopharyngeal Neoplasms, Neoplastic Syndromes, Hereditary/diagnosis, article

URL: https://curis.ku.dk/portal/da/publications/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypperTest(e406d31e-3055-44bc-887a-bd4d5d0d9cee).html
https://curis.ku.dk/ws/files/337983106/v02210148_web.pdfTest
https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2022-03/v02210148_web.pdfTest

عناروين إضافية: GUIDELINES FOR THE DIAGNOSIS AND TREATMENT OF HEREDITARY ANGIOEDEMA

المصدر: Liječnički vjesnik; ISSN 0024-3477 (Print); ISSN 1849-2177 (Online); Volume 136; Issue 5-6

مصطلحات الفهرس: Hereditarni angioedem – dijagnoza, patofiziologija, farmakoterapija, prevencija; Protein inhibitor C1 – analiza, terapijska primjena; Komplement C1 – antagonisti i inhibitori; Bradikininski B2 receptor – antagonisti i inhibitori; Bradikinin – analozi i derivati; Smjernice; Hrvatska, Angioedemas, hereditary – diagnosis, physiopathology, drug therapy, prevention and control; Complement C1 inhibitor protein – analysis, therapeutic use, administration and dosage; Complement C1 – antagonists and inhibitors; Receptor, bradykinin B2 – antagonists and inhibitors; Bradykinin – analogs and derivatives; Practice guidelines as topic; Croatia, text, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion

URL: https://hrcak.srce.hr/172600Test
https://hrcak.srce.hr/file/254682Test

المصدر: Clinical chemistry and laboratory medicine, 49 (3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Electrophoresis, Polyacrylamide Gel, Erythrocyte Membrane -- chemistry, Erythrocytes -- chemistry, Humans, Membrane Proteins -- analysis, Spherocytosis, Hereditary -- diagnosis, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/156655Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Clinical chemistry and laboratory medicine, 49 (3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Electrophoresis, Polyacrylamide Gel, Erythrocyte Membrane -- chemistry, Erythrocytes -- chemistry, Humans, Membrane Proteins -- analysis, Spherocytosis, Hereditary -- diagnosis, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/156655Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Orphanet journal of rare diseases, 3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Audiometry, Child, Child, Preschool, Corneal Dystrophies, Hereditary -- diagnosis, Corneal Dystrophies, Hereditary -- genetics, Corneal Dystrophies, Hereditary -- physiopathology, Corneal Dystrophies, Hereditary -- surgery, Corneal Transplantation, Female, Hearing Loss, Sensorineural -- diagnosis, Hearing Loss, Sensorineural -- genetics, Hearing Loss, Sensorineural -- physiopathology, Hearing Loss, Sensorineural -- surgery, Humans, Male, Young Adult, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: https://dipot.ulb.ac.be/dspace/bitstream/2013/53602/4/doi_28927.pdfTest
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53602Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Orphanet journal of rare diseases, 3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Audiometry, Child, Child, Preschool, Corneal Dystrophies, Hereditary -- diagnosis, Corneal Dystrophies, Hereditary -- genetics, Corneal Dystrophies, Hereditary -- physiopathology, Corneal Dystrophies, Hereditary -- surgery, Corneal Transplantation, Female, Hearing Loss, Sensorineural -- diagnosis, Hearing Loss, Sensorineural -- genetics, Hearing Loss, Sensorineural -- physiopathology, Hearing Loss, Sensorineural -- surgery, Humans, Male, Young Adult, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: https://dipot.ulb.ac.be/dspace/bitstream/2013/53602/4/doi_28927.pdfTest
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53602Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Panminerva medica, 48 (3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adenosine Triphosphatases -- genetics, Adult, Aged, Cytosine, Exons, Female, Genes, Dominant, Humans, Italy, Leucine, Magnetic Resonance Imaging, Male, Mutation, Missense, Proline, Spastic Paraplegia, Hereditary -- diagnosis, Spastic Paraplegia, Hereditary -- genetics, Thymine, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51423Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Panminerva medica, 48 (3

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adenosine Triphosphatases -- genetics, Adult, Aged, Cytosine, Exons, Female, Genes, Dominant, Humans, Italy, Leucine, Magnetic Resonance Imaging, Male, Mutation, Missense, Proline, Spastic Paraplegia, Hereditary -- diagnosis, Spastic Paraplegia, Hereditary -- genetics, Thymine, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51423Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Bulletin de la Société belge d'ophtalmologie, 243

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Child, DNA -- genetics, DNA, Antisense -- isolation & purification, Female, Humans, Male, Mutation, Optic Atrophies, Hereditary -- diagnosis, Optic Atrophies, Hereditary -- genetics, Polymerase Chain Reaction, Visual Acuity, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/57902Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest