المؤلفون: Michal M; Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic.; Bioptic Laboratory, Ltd, Plzen, Czech Republic.; Cytopathos, Ltd., Bratislava, Slovak Republic., Skálová A; Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic.; Bioptic Laboratory, Ltd, Plzen, Czech Republic., Hyrcza M; Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Canada., Laco J; The Fingerland Department of Pathology, Faculty of Medicine, Charles University, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic., Vaněček T; Bioptic Laboratory, Ltd, Plzen, Czech Republic., Rupp NJ; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland., Michal M; Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic.; Bioptic Laboratory, Ltd, Plzen, Czech Republic., Michalová K; Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic.; Bioptic Laboratory, Ltd, Plzen, Czech Republic., Agaimy A; Institute of Pathology, Friedrich-Alexander University of Erlangen-Nuremberg, University Hospital of Erlangen, Erlangen, Germany., Bradová M; Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic. bradova@biopticka.cz.; Bioptic Laboratory, Ltd, Plzen, Czech Republic. bradova@biopticka.cz.

المصدر: Virchows Archiv : an international journal of pathology [Virchows Arch] 2024 Jul; Vol. 485 (1), pp. 31-42. Date of Electronic Publication: 2023 Dec 13.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer International Country of Publication: Germany NLM ID: 9423843 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-2307 (Electronic) Linking ISSN: 09456317 NLM ISO Abbreviation: Virchows Arch Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma*/pathology , Hamartoma*/genetics, Humans ; Male ; Female ; Middle Aged ; Aged ; Adult ; Nose Neoplasms/pathology ; Nose Neoplasms/genetics ; Mutation ; Adenoma/pathology ; Adenoma/genetics ; Paranasal Sinus Neoplasms/pathology ; Paranasal Sinus Neoplasms/genetics ; Respiratory Mucosa/pathology ; Aged, 80 and over

المؤلفون: Rajeswarie RT; Department of Laboratory Medicine - Histopathology, Sakra World Hospital, Bengaluru, Karnataka, India., Mallik D; Departments of Laboratory Medicine and Neurosurgery, Sakra World Hospital, Bangalore, Karnataka, India.; Department of Neuroscience, Sakra World Hospital, Bengaluru, Karnataka, India., Gopal S; Departments of Laboratory Medicine and Neurosurgery, Sakra World Hospital, Bangalore, Karnataka, India.

المصدر: International journal of surgical pathology [Int J Surg Pathol] 2024 Sep; Vol. 32 (6), pp. 1113-1116. Date of Electronic Publication: 2023 Dec 10.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Sage Publications Country of Publication: United States NLM ID: 9314927 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1940-2465 (Electronic) Linking ISSN: 10668969 NLM ISO Abbreviation: Int J Surg Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma Syndrome, Multiple*/pathology , Hamartoma Syndrome, Multiple*/diagnosis, Adult ; Female ; Humans

المؤلفون: Al-Ramadhani R; Department of Pediatric Neurology, Emory University School of Medicine, Atlanta, Georgia; Department of Pediatric Neurology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania., Bhalla S; Department of Pediatric Neurology, Emory University School of Medicine, Atlanta, Georgia; Department of Pediatric Neurology, Children's Healthcare of Atlanta, Atlanta, Georgia. Electronic address: Sonam.bhalla@emory.edu., Bearden DJ; Department of Pediatric Neurology, Emory University School of Medicine, Atlanta, Georgia; Department of Pediatric Neuropsychology, Children's Healthcare of Atlanta, Atlanta, Georgia., Ono K; Department of Pediatric Neuropsychology, Children's Healthcare of Atlanta, Atlanta, Georgia., Chern J; Department of Pediatric Neurosurgery, Children's Healthcare of Atlanta, Atlanta, Georgia., Kheder A; Department of Pediatric Neurology, Emory University School of Medicine, Atlanta, Georgia; Department of Pediatric Neurology, Children's Healthcare of Atlanta, Atlanta, Georgia.

المصدر: Pediatric neurology [Pediatr Neurol] 2024 Sep; Vol. 158, pp. 11-16. Date of Electronic Publication: 2024 May 19.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Elsevier Science Publishing Country of Publication: United States NLM ID: 8508183 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5150 (Electronic) Linking ISSN: 08878994 NLM ISO Abbreviation: Pediatr Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma*/complications , Hamartoma*/surgery , Hamartoma*/physiopathology , Hypothalamic Diseases*/complications , Hypothalamic Diseases*/surgery , Hypothalamic Diseases*/physiopathology , Hypothalamic Diseases*/diagnosis , Hypothalamic Diseases*/diagnostic imaging , Seizures*/etiology , Seizures*/physiopathology , Seizures*/surgery , Seizures*/diagnostic imaging, Humans ; Male ; Child, Preschool ; Cerebral Cortex/diagnostic imaging ; Cerebral Cortex/physiopathology ; Cerebral Cortex/pathology ; Cerebral Cortex/surgery ; Electroencephalography ; Laser Therapy

SCR Disease Name: Hypothalamic hamartomas

المؤلفون: Mackay G; Department of Health Science, The University of Auckland Faculty of Medical and Health Sciences, Auckland, New Zealand., Johnston J; Department of Surgery, The University of Auckland, Auckland, New Zealand., Mallick S; Department of ORL Head and Neck Surgery, Auckland District Health Board, Auckland, New Zealand., Khanijow V; Department of Pathology, Auckland City Hospital, Auckland, New Zealand.

المصدر: International journal of surgical pathology [Int J Surg Pathol] 2024 Sep; Vol. 32 (6), pp. 1129-1133. Date of Electronic Publication: 2023 Nov 20.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Sage Publications Country of Publication: United States NLM ID: 9314927 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1940-2465 (Electronic) Linking ISSN: 10668969 NLM ISO Abbreviation: Int J Surg Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma*/pathology , Hamartoma*/diagnosis , Hamartoma*/surgery , Magnetic Resonance Imaging*, Humans ; Middle Aged ; Female ; Lymph Nodes/pathology ; Neck/pathology ; Angiomyoma/pathology ; Angiomyoma/diagnosis ; Angiomyoma/surgery

المؤلفون: Drissen MMCM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands., Vos JR; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands., Collado Camps E; Department of Tumour Immunology, Radboud University Medical Center, Nijmegen, the Netherlands., Schuurs-Hoeijmakers JHM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands., Schieving JH; Department of Paediatric Neurology, Radboud University Medical Center, Nijmegen, the Netherlands., Hoogerbrugge N; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: Nicoline.Hoogerbrugge@radboudumc.nl.

المصدر: European journal of medical genetics [Eur J Med Genet] 2024 Aug; Vol. 70, pp. 104960. Date of Electronic Publication: 2024 Jul 21.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Autoimmune Diseases*/genetics , Hamartoma Syndrome, Multiple*/genetics , Hamartoma Syndrome, Multiple*/pathology , Hamartoma Syndrome, Multiple*/complications, Adult ; Child ; Child, Preschool ; Female ; Humans ; Male ; Middle Aged ; Infections ; PTEN Phosphohydrolase/genetics ; Retrospective Studies

المؤلفون: Luisi C; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Salimbene L; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Pietrafusa N; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Trivisano M; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Marras CE; Neurosurgery Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., De Benedictis A; Neurosurgery Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Chiarello D; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Mercier M; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Pepi C; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., de Palma L; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy., Specchio N; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network on Rare and Complex Epilepsies, EpiCARE, Rome, Italy. Electronic address: nicola.specchio@opbg.net.

المصدر: Epilepsy & behavior : E&B [Epilepsy Behav] 2024 Aug; Vol. 157, pp. 109846. Date of Electronic Publication: 2024 May 30.

نوع المنشور: Systematic Review; Journal Article

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 100892858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-5069 (Electronic) Linking ISSN: 15255050 NLM ISO Abbreviation: Epilepsy Behav Subsets: MEDLINE

مواضيع طبية MeSH: Hypothalamic Diseases*/surgery , Hypothalamic Diseases*/complications , Hamartoma*/surgery , Hamartoma*/complications , Epilepsy*/surgery , Epilepsy*/psychology, Humans ; Treatment Outcome ; Neurosurgical Procedures/adverse effects ; Neuropsychological Tests ; Postoperative Complications/etiology ; Postoperative Complications/psychology ; Mental Disorders/etiology

SCR Disease Name: Hypothalamic hamartomas

المؤلفون: MacFarland SP; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA., Duvall M; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Kemajou RT; Eastern Virginia Medical School, Norfolk, Virginia, USA., Baldino SE; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Zelley K; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Black C; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Behavioral Neuroscience Core, Center for Human Phenomic Science, The Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania, USA., Thomas A; Behavioral Neuroscience Core, Center for Human Phenomic Science, The Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania, USA., Thomas NH; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Behavioral Neuroscience Core, Center for Human Phenomic Science, The Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania, USA., Ruffner M; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA., Li Y; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA., Miller JS; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA., Brodeur GM; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA., Shabason E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Children's Hospital of Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Aug; Vol. 194 (8), pp. e63608. Date of Electronic Publication: 2024 Mar 28.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Phenotype* , Hamartoma Syndrome, Multiple*/genetics , Hamartoma Syndrome, Multiple*/pathology , Hamartoma Syndrome, Multiple*/diagnosis , Autism Spectrum Disorder*/genetics , Autism Spectrum Disorder*/pathology , Autism Spectrum Disorder*/epidemiology , Autism Spectrum Disorder*/diagnosis , PTEN Phosphohydrolase*/genetics, Humans ; Male ; Female ; Child ; Adolescent ; Child, Preschool ; Quality of Life

المؤلفون: Cao C; Department of Orthopaedic Surgery, Yongchuan Hospital of Chongqing Medical University, Chongqing, China., Li Q; Department of neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing, China., Dong J; Department of Clinical Medicine, Chongqing Medical and Pharmaceutical College, Chongqing, China. Electronic address: tokyo2024@126.com., Lu M; Department of Pain Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

المصدر: World neurosurgery [World Neurosurg] 2024 Jul; Vol. 187, pp. e792-e797. Date of Electronic Publication: 2024 May 03.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101528275 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-8769 (Electronic) Linking ISSN: 18788750 NLM ISO Abbreviation: World Neurosurg Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma*/surgery , Hamartoma*/diagnostic imaging , Magnetic Resonance Imaging*, Humans ; Female ; Male ; Adult ; Middle Aged ; Treatment Outcome ; Retrospective Studies ; Young Adult ; Neurosurgical Procedures/methods ; Adolescent

المؤلفون: Drozdz W; Department of Internal Medicine, Kantonsspital Graubünden, Chur, Graubünden, Switzerland., Joller D; Department of Internal Medicine, Kantonsspital Graubünden, Chur, Graubünden, Switzerland., Grosse P; Department of Internal Medicine, Kantonsspital Graubünden, Chur, Graubünden, Switzerland., Fehr T; Department of Internal Medicine, Kantonsspital Graubünden, Chur, Graubünden, Switzerland Thomas.fehr@ksgr.ch.

المصدر: BMJ case reports [BMJ Case Rep] 2024 Sep 12; Vol. 17 (9). Date of Electronic Publication: 2024 Sep 12.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: PTEN Phosphohydrolase*/genetics , Hamartoma Syndrome, Multiple*/genetics , Hamartoma Syndrome, Multiple*/complications , Lupus Nephritis*/genetics , Lupus Nephritis*/complications, Humans ; Male ; Mutation ; Adult

المؤلفون: Kapačinskaitė M; Faculty of Medicine, Vilnius University, M.K. Čiurlionio g. 21, 03101, Vilnius, Lithuania. medeine.kapac@gmail.com., Stratica N; University of Medicine and Pharmacy 'Grigore T. Popa', Strada Universității 16, 700115, Iași, Romania., Adomaitienė I; Center for Pediatric Oncology and Hematology, Vilnius University Hospital Santaros Klinikos, Santariskiu 24, 08406, Vilnius, Lithuania., Rascon J; Clinic of Pediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Vaišnytė B; Faculty of Medicine, Vilnius University, M.K. Čiurlionio g. 21, 03101, Vilnius, Lithuania.; Center of Vascular and Endovascular Surgery, Vilnius University Hospital Santaros Klinikos, Santariskiu 2, 08406, Vilnius, Lithuania.

المصدر: Scientific reports [Sci Rep] 2024 Sep 10; Vol. 14 (1), pp. 21119. Date of Electronic Publication: 2024 Sep 10.

نوع المنشور: Systematic Review; Journal Article

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma Syndrome, Multiple*/genetics , Hamartoma Syndrome, Multiple*/pathology , Hamartoma Syndrome, Multiple*/diagnosis , PTEN Phosphohydrolase*/genetics, Humans ; Child ; Female ; Male ; Child, Preschool ; Adolescent ; Infant