المؤلفون: Tam OCH; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong., Ho RSL; Department of Pathology, Gleneagles Hospital, Wong Chuk Hang, Hong Kong., Chan S; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong., Li KKW; Department of Anatomical and Cellular Pathology, Chinese University of Hong Kong, Sha Tin, Hong Kong., Lam TL; Department of Pathology, Queen Elizabeth Hospital, Kowloon, Hong Kong., Cheung ETY; Department of Pathology, Queen Elizabeth Hospital, Kowloon, Hong Kong., Cheung OY; Department of Pathology, Queen Elizabeth Hospital, Kowloon, Hong Kong., Ho WWS; Department of Neurosurgery, Queen Mary Hospital, Pok Fu Lam, Hong Kong.; Department of Neurosurgery, Hong Kong Children's Hospital, Kowloon, Hong Kong., Cheng KKF; Department of Neurosurgery, Queen Mary Hospital, Pok Fu Lam, Hong Kong.; Department of Neurosurgery, Hong Kong Children's Hospital, Kowloon, Hong Kong., Shing MMK; Department of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Kowloon, Hong Kong., Ku DTL; Department of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Kowloon, Hong Kong., Chung BHY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong., Yang W; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong., Chan GCF; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.; Department of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Kowloon, Hong Kong., Ng HK; Department of Anatomical and Cellular Pathology, Chinese University of Hong Kong, Sha Tin, Hong Kong., Liu APY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.; Department of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Kowloon, Hong Kong.

المصدر: Cancers [Cancers (Basel)] 2023 Oct 07; Vol. 15 (19). Date of Electronic Publication: 2023 Oct 07.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101526829 Publication Model: Electronic Cited Medium: Print ISSN: 2072-6694 (Print) Linking ISSN: 20726694 NLM ISO Abbreviation: Cancers (Basel) Subsets: PubMed not MEDLINE

المؤلفون: Wong CF; Grantham Hospital, TB and Chest Unit. wongcf2001@yahoo.com.hk., Yan SW, Wong WM, Ho RSL

المصدر: Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace [Monaldi Arch Chest Dis] 2018 Sep 07; Vol. 88 (3), pp. 922. Date of Electronic Publication: 2018 Sep 07.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Fondazione clinica del lavoro edizioni : Distributed by PI-ME tipographia Country of Publication: Italy NLM ID: 9307314 Publication Model: Electronic Cited Medium: Print ISSN: 1122-0643 (Print) Linking ISSN: 11220643 NLM ISO Abbreviation: Monaldi Arch Chest Dis Subsets: MEDLINE

مواضيع طبية MeSH: Complementary Therapies* , Oils*, Pneumonia, Lipid/*diagnostic imaging, Bronchoalveolar Lavage Fluid ; Carcinoma ; Enteral Nutrition ; Female ; Gastrostomy ; Humans ; Middle Aged ; Pneumonia, Lipid/diagnosis ; Tomography, X-Ray Computed ; Tongue Neoplasms

المؤلفون: Donkervoort S; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Chan SHS; Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR., Hayes LH; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA; Boston Children's Hospital, Boston, MA, USA., Bradley N; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Nguyen D; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Leach ME; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA; Children's National Health System, Washington, DC, USA., Mohassel P; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Hu Y; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Thangarajh M; Children's National Health System, Washington, DC, USA., Bharucha-Goebel D; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA; Children's National Health System, Washington, DC, USA., Kan A; Department of Pathology and Clinical Biochemistry, The Queen Mary Hospital, Hong Kong SAR., Ho RSL; Department of Pathology and Clinical Biochemistry, The Queen Mary Hospital, Hong Kong SAR., Reyes CA; Children's National Health System, Washington, DC, USA., Nance J; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Moore SA; Department of Pathology, University of Iowa Carver College of Medicine, Iowa City, IA, USA., Foley AR; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA., Bönnemann CG; National Institutes of Health, Neuromuscular and Neurogenetic Disorders of Childhood Section, Bethesda, MD, USA. Electronic address: carsten.bonnemann@nih.gov.

المصدر: Neuromuscular disorders : NMD [Neuromuscul Disord] 2017 Jun; Vol. 27 (6), pp. 531-536. Date of Electronic Publication: 2017 Mar 02.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Pergamon Press Country of Publication: England NLM ID: 9111470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2364 (Electronic) Linking ISSN: 09608966 NLM ISO Abbreviation: Neuromuscul Disord Subsets: MEDLINE

مواضيع طبية MeSH: Actins/*genetics , Inclusion Bodies/*pathology , Muscular Diseases/*genetics , Muscular Diseases/*pathology , Myopathies, Nemaline/*genetics , Myopathies, Nemaline/*pathology, Child, Preschool ; Humans ; Male ; Muscle, Skeletal/pathology ; Muscular Diseases/complications ; Mutation ; Myopathies, Nemaline/complications ; Pedigree ; Twins ; Exome Sequencing