المؤلفون: Burke AB; Department of Oral and Maxillofacial Surgery, University of Washington School of Dentistry, 1959 Northeast Pacific Street, Box 357134, Seattle, WA 98195-7134, USA. Electronic address: abburke@uw.edu.

المصدر: Oral and maxillofacial surgery clinics of North America [Oral Maxillofac Surg Clin North Am] 2024 Aug; Vol. 36 (3), pp. 379-390. Date of Electronic Publication: 2024 May 04.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: W.B. Saunders Co Country of Publication: United States NLM ID: 9001454 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1365 (Electronic) Linking ISSN: 10423699 NLM ISO Abbreviation: Oral Maxillofac Surg Clin North Am Subsets: MEDLINE

مواضيع طبية MeSH: Fibrous Dysplasia of Bone*/diagnostic imaging , Fibrous Dysplasia of Bone*/diagnosis, Humans ; Child ; Diagnosis, Differential ; Facial Bones ; Fibroma, Ossifying/diagnosis ; Fibroma, Ossifying/surgery ; Craniofacial Fibrous Dysplasia/diagnosis ; Craniofacial Fibrous Dysplasia/pathology ; Skull Neoplasms/diagnostic imaging ; Skull Neoplasms/diagnosis ; Skull Neoplasms/pathology

عنوان ترانسليتريتد: Fibröse Dysplasie.

المؤلفون: Waltermann A; Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland., Westhoff B; Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland. Westhoff@med.uni-duesseldorf.de.

المصدر: Orthopadie (Heidelberg, Germany) [Orthopadie (Heidelb)] 2024 Oct; Vol. 53 (10), pp. 805-816. Date of Electronic Publication: 2024 Sep 05.

نوع المنشور: Journal Article; English Abstract; Review

بيانات الدورية: Publisher: Springer Medizin Country of Publication: Germany NLM ID: 9918384887206676 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2731-7153 (Electronic) Linking ISSN: 27317145 NLM ISO Abbreviation: Orthopadie (Heidelb) Subsets: MEDLINE

مواضيع طبية MeSH: Fibrous Dysplasia of Bone*/diagnosis , Fibrous Dysplasia of Bone*/pathology, Humans ; Fibrous Dysplasia, Polyostotic/pathology ; Fibrous Dysplasia, Polyostotic/diagnosis ; Fibrous Dysplasia, Polyostotic/therapy

المؤلفون: Haydel A; Department of Orthopaedics, LSUHSC School of Medicine, New Orleans, LA, USA., Craver R; Department of Pathology, Children's Hospital of New Orleans, New Orleans, LO, USA., Cable M; Department of Orthopaedics, LSUHSC School of Medicine, New Orleans, LA, USA.

المصدر: Fetal and pediatric pathology [Fetal Pediatr Pathol] 2024 May-Jun; Vol. 43 (3), pp. 214-224. Date of Electronic Publication: 2024 Apr 08.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 101230972 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1551-3823 (Electronic) Linking ISSN: 15513815 NLM ISO Abbreviation: Fetal Pediatr Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Fibrous Dysplasia, Polyostotic*/diagnosis , Fibrous Dysplasia, Polyostotic*/complications , Femur*/pathology, Humans ; Female ; Male ; Fractures, Spontaneous/etiology ; Fractures, Spontaneous/diagnosis ; Child ; Diagnosis, Differential ; Fibrous Dysplasia of Bone/diagnosis ; Fibrous Dysplasia of Bone/complications ; Fibrous Dysplasia of Bone/pathology

المؤلفون: Cantini JE; University Foundation of Health Sciences-FUCS, Hospital de San José. Bogota, Colombia., Vergel MF; Fundación Universitaria de Ciencias de la Salud-FUCS, Hospital de San José. Bogota, Colombia., Tapiero X; Fundación Universitaria de Ciencias de la Salud-FUCS, Hospital de San José. Bogotá, Colombia., Gómez-Ortega V; Burn Unit of the Fundación Santa Fe de Bogota, Colombia.

المصدر: The Journal of craniofacial surgery [J Craniofac Surg] 2024 Jun 01; Vol. 35 (4), pp. 1177-1180. Date of Electronic Publication: 2024 Apr 03.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9010410 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1536-3732 (Electronic) Linking ISSN: 10492275 NLM ISO Abbreviation: J Craniofac Surg Subsets: MEDLINE

مواضيع طبية MeSH: Craniofacial Fibrous Dysplasia*/surgery, Humans ; Colombia ; Male ; Female ; Retrospective Studies ; Adolescent ; Adult ; Child ; Treatment Outcome ; Plastic Surgery Procedures/methods ; Fibrous Dysplasia, Monostotic/surgery ; Fibrous Dysplasia, Polyostotic/surgery ; Young Adult ; Middle Aged

المؤلفون: Nagayama S; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan., Takahashi H; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan., Hasegawa F; Department of Clinical Genetics, National Center for Child Health and Development, Tokyo, Japan., Hori A; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan., Kizami S; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan., Furukawa R; Department of Radiology, Jichi Medical University, Shimotsuke, Japan., Horie K; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan., Ogoyama M; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan., Hata K; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan.; Department of Molecular Biology, Gunma University, Maebashi, Japan., Fujiwara H; Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, Japan.

المصدر: Congenital anomalies [Congenit Anom (Kyoto)] 2024 Jul; Vol. 64 (4), pp. 177-181. Date of Electronic Publication: 2024 Apr 18.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley on behalf of the Japanese Teratology Society Country of Publication: Australia NLM ID: 9306292 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1741-4520 (Electronic) Linking ISSN: 09143505 NLM ISO Abbreviation: Congenit Anom (Kyoto) Subsets: MEDLINE

مواضيع طبية MeSH: Phenotype* , Ectodermal Dysplasia*/genetics , Ectodermal Dysplasia*/diagnosis , Ectodermal Dysplasia*/pathology , Exome Sequencing*, Humans ; Female ; Pregnancy ; Adult ; Ultrasonography, Prenatal ; Mutation ; Heterozygote ; Bone and Bones/abnormalities ; Craniosynostoses

SCR Disease Name: Cranioectodermal Dysplasia

المؤلفون: Hande A; Department of Oral & Maxillofacial Pathology and Microbiology, Sharad Pawar Dental College & Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, 442004, Maharashtra, India., Kalmegh P; Department of Oral & Maxillofacial Pathology and Microbiology, Sharad Pawar Dental College & Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, 442004, Maharashtra, India. padmashrikalmegh16@gmail.com., Patil S; Department of Oral & Maxillofacial Pathology and Microbiology, Sharad Pawar Dental College & Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, 442004, Maharashtra, India., Sonone A; Department of Oral & Maxillofacial Pathology and Microbiology, Sharad Pawar Dental College & Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, 442004, Maharashtra, India., Pakhale A; Department of Oral & Maxillofacial Pathology and Microbiology, Sharad Pawar Dental College & Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, 442004, Maharashtra, India.

المصدر: BMC oral health [BMC Oral Health] 2024 Sep 19; Vol. 24 (1), pp. 1119. Date of Electronic Publication: 2024 Sep 19.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101088684 Publication Model: Electronic Cited Medium: Internet ISSN: 1472-6831 (Electronic) Linking ISSN: 14726831 NLM ISO Abbreviation: BMC Oral Health Subsets: MEDLINE

مواضيع طبية MeSH: Fibrous Dysplasia, Monostotic*/diagnostic imaging , Fibrous Dysplasia, Monostotic*/pathology, Humans ; Female ; Male ; Retrospective Studies ; Adolescent ; Child ; Adult ; Jaw Diseases/diagnostic imaging ; Jaw Diseases/pathology ; Young Adult

المؤلفون: Yan C; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Gong X; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Luo H; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Liu Y; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Lin Y; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Weng B; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China., Cai C; Department of Neonatology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. caic@shchildren.com.cn.

المصدر: Italian journal of pediatrics [Ital J Pediatr] 2024 Sep 16; Vol. 50 (1), pp. 178. Date of Electronic Publication: 2024 Sep 16.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium: Internet ISSN: 1824-7288 (Electronic) Linking ISSN: 17208424 NLM ISO Abbreviation: Ital J Pediatr Subsets: MEDLINE

مواضيع طبية MeSH: Bronchopulmonary Dysplasia*/epidemiology , Bronchopulmonary Dysplasia*/therapy , Respiratory Distress Syndrome, Newborn*/therapy, Humans ; Infant, Newborn ; Female ; Retrospective Studies ; Male ; Practice Guidelines as Topic ; Incidence ; Respiration, Artificial ; Infant, Premature ; Europe ; Infant, Extremely Premature

المؤلفون: Avitabile CM; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Echocardiography Laboratory Research Unit, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. Electronic address: avitabilec@chop.edu., Zhang X; Data Science and Biostatistics Unit, Department of Biomedical and Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Ampah S; Data Science and Biostatistics Unit, Department of Biomedical and Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Wang Y; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Echocardiography Laboratory Research Unit, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Ash D; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Echocardiography Laboratory Research Unit, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Nilan K; Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Tingo JE; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Frank DB; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Jensen EA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA; Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Lingappan K; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA; Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA., Gibbs KA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA; Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

المصدر: International journal of cardiology [Int J Cardiol] 2024 Sep 15; Vol. 411, pp. 132246. Date of Electronic Publication: 2024 Jun 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 8200291 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1874-1754 (Electronic) Linking ISSN: 01675273 NLM ISO Abbreviation: Int J Cardiol Subsets: MEDLINE

مواضيع طبية MeSH: Bronchopulmonary Dysplasia*/physiopathology , Bronchopulmonary Dysplasia*/diagnosis , Pulmonary Wedge Pressure*/physiology , Cardiac Catheterization*, Humans ; Retrospective Studies ; Male ; Female ; Infant ; Blood Pressure/physiology ; Cohort Studies ; Infant, Newborn ; Echocardiography/methods

المؤلفون: Pang H; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China., Xu L; Department of Orthopaedic Surgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, China., Su F; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China., Li M; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China., Dang Y; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China., Wang B; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China., Jie Q; Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, China. jieqiangchina@126.com.

المصدر: Scientific reports [Sci Rep] 2024 Sep 12; Vol. 14 (1), pp. 21363. Date of Electronic Publication: 2024 Sep 12.

نوع المنشور: 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: Developmental Dysplasia of the Hip*/diagnostic imaging , Developmental Dysplasia of the Hip*/pathology , Femur Head Necrosis*/etiology , Femur Head Necrosis*/pathology , Femur Head Necrosis*/diagnostic imaging , Magnetic Resonance Imaging*, Humans ; Male ; Female ; Risk Factors ; Infant ; Postoperative Complications/etiology ; Child, Preschool ; Child ; Retrospective Studies ; Hip Dislocation, Congenital/complications ; Hip Dislocation, Congenital/surgery ; Hip Dislocation, Congenital/diagnostic imaging

المؤلفون: Kim MJ; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea., Lee JS; Department of Laboratory Medicine, Seoul National University Hospital, 101, Daehak-ro, Jongno-gu, Seoul, 110-744, Korea., Chae SW; Department of Laboratory Medicine, Seoul National University Hospital, 101, Daehak-ro, Jongno-gu, Seoul, 110-744, Korea.; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea., Cho SI; Department of Laboratory Medicine, Seoul National University Hospital, 101, Daehak-ro, Jongno-gu, Seoul, 110-744, Korea., Moon J; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea., Ko JM; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea., Chae JH; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea., Seong MW; Department of Laboratory Medicine, Seoul National University Hospital, 101, Daehak-ro, Jongno-gu, Seoul, 110-744, Korea. mwseong@snu.ac.kr.; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea. mwseong@snu.ac.kr.

المصدر: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Sep 07; Vol. 19 (1), pp. 329. Date of Electronic Publication: 2024 Sep 07.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

مواضيع طبية MeSH: Ectodermal Dysplasia*/genetics , Ectodermal Dysplasia*/diagnosis , Exome Sequencing*/methods , Mutation*/genetics, Humans ; Republic of Korea ; Male ; Female ; Child ; DNA Copy Number Variations/genetics ; Genetic Profile ; Child, Preschool ; Adult ; Adolescent ; Edar Receptor/genetics ; Ectodysplasins/genetics ; Infant ; Young Adult