WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts von Kantaputra, Piranit Nik, Sirirungruangsarn, Yuddhasert, Visrutaratna, Pannee, Petcharunpaisan, Sasitorn, Carlson, Bruce M, Intachai, Worrachet, Sudasna, Jutamas, Kampuansai, Jatupol, Dejkhamron, Prapai

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Pheochromocytoma presenting with QT prolongation and catecholamine-induced myocarditis in a child von Saengsin, Kwannapas, Sethasathien, Saviga, Dejkhamron, Prapai, Sittiwangkul, Rekwan, Makonkawkeyoon, Krit, Silvilairat, Suchaya, Wejaphikul, Karn, Pongprot, Yupada

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Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation von Kantaputra, Piranit Nik, Sirirungruangsarn, Yuddhasert, Intachai, Worrachet, Ngamphiw, Chumpol, Tongsima, Sissades, Dejkhamron, Prapai

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Enamel-renal-gingival syndrome and FAM20A mutations von Kantaputra, Piranit Nik, Kaewgahya, Massupa, Khemaleelakul, Udomrat, Dejkhamron, Prapai, Sutthimethakorn, Suchitra, Thongboonkerd, Visith, Iamaroon, Anak

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Subtle inflammation: a possible mechanism of future cardiovascular risk in obese children von Sontichai, Watchareewan, Dejkhamron, Prapai, Pothacharoen, Peraphan, Kongtaweelert, Prachya, Unachak, Kevalee, Ukarapol, Nuthapong

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Potential Role of Sleep Disturbance in the Development of Early Puberty: Past Clinical Evidence for Future Management von Puttawong, Dolrutai, Wejaphikul, Karn, Thonusin, Chanisa, Dejkhamron, Prapai, Chattipakorn, Nipon, Chattipakorn, Siriporn C.

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Novel Variants and Phenotypes in NEUROG3-Associated Syndrome von Wejaphikul, Karn, Srilanchakon, Khomsak, Kamolvisit, Wuttichart, Jantasuwan, Supavadee, Santawong, Kanokwan, Tongkobpetch, Siraprapa, Theerapanon, Thanakorn, Damrongmanee, Alisara, Hongsawong, Nattaphorn, Ukarapol, Nuthapong, Dejkhamron, Prapai, Supornsilchai, Vichit, Porntaveetus, Thantrira, Shotelersuk, Vorasuk

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Effects of gentamicin inducing readthrough premature stop Codons: A study of alpha-L-iduronidase nonsense variants in COS-7 Cells von Ngiwsara, Lukana, Sawangareetrakul, Phannee, Wattanasirichaigoon, Duangrurdee, Tim-Aroon, Thipwimol, Dejkhamron, Prapai, Champattanachai, Voraratt, Ketudat-Cairns, James R., Svasti, Jisnuson

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Pregnancy Outcomes among Women with Graves’ Hyperthyroidism: A Retrospective Cohort Study von Harn-a-morn, Panwad, Dejkhamron, Prapai, Tongsong, Theera, Luewan, Suchaya

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A Novel GNAS Mutation Causing Isolated Infantile Cushing’s Syndrome von Dejkhamron, Prapai, Ittiwut, Chupong, TangNgam, Hataitip, Sunkonkit, Kanokkarn, Natesirinilkul, Rungrote, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk

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Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation von Wejaphikul, Karn, Dejkhamron, Prapai, Khorana, Jiraporn, Watcharachan, Kirati, Intachai, Worrachet, Olsen, Bjorn, Tongsima, Sissades, Ketudat Cairns, James R., Ngamphiw, Chumpol, Kantaputra, Piranit

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Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations von Kantaputra, Piranit, Dejkhamron, Prapai, Sittiwangkul, Rekwan, Katanyuwong, Kamornwan, Ngamphiw, Chumpol, Sonsuwan, Nuntigar, Intachai, Worrachet, Tongsima, Sissades, Beales, Philip L, Buranaphatthana, Worakanya

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Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2 von Kantaputra, Piranit Nik, Dejkhamron, Prapai, Intachai, Worrachet, Ngamphiw, Chumpol, Kawasaki, Katsushige, Ohazama, Atsushi, Krisanaprakornkit, Suttichai, Olsen, Bjorn, Tongsima, Sissades, Ketudat Cairns, Jame R

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Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2 von Kantaputra, Piranit Nik, Dejkhamron, Prapai, Tongsima, Sissades, Ngamphiw, Chumpol, Intachai, Worrachet, Ngiwsara, Lukana, Sawangareetrakul, Phannee, Svasti, Jisnuson, Olsen, Bjorn, Cairns, James R. Ketudat, Bumroongkit, Kanokkan

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Role of Leucine 341 in Thyroid Hormone Receptor Beta Revealed by a Novel Mutation Causing Thyroid Hormone Resistance von Wejaphikul, Karn, Groeneweg, Stefan, Dejkhamron, Prapai, Unachak, Kevalee, Visser, W. Edward, Chatterjee, V. Krishna, Visser, Theo J., Meima, Marcel E., Peeters, Robin P.

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Inhibition of Growth Hormone Receptor Gene Expression by Saturated Fatty Acids: Role of Krüppel-Like Zinc Finger Factor, ZBP-89 von Thimmarayappa, Jamuna, Sun, Jinhong, Schultz, Laura E, Dejkhamron, Prapai, Lu, Chunxia, Giallongo, Agata, Merchant, Juanita L, Menon, Ram K

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Local anthropometric parameters for assessing double burden of malnutrition in South Asian and Southeast Asian countries: a review and retrospective analysis von Khadilkar, Anuradha V., Oza, Chirantap, Kajale, Neha, Pulungan, Aman B., Wacharasindhu, Suttipong, Moelyo, Annang Giri, Amalia, Gassani, Wejaphikul, Karn, Julia, Madarina, Dejkhamron, Prapai, Khadilkar, Vaman

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A Longitudinal Study of Growth and Relation With Anemia and Iron Overload in Pediatric Patients With Transfusion-dependent Thalassemia von Nokeaingtong, Kwannapas, Charoenkwan, Pimlak, Silvilairat, Suchaya, Saekho, Suwit, Pongprot, Yupada, Dejkhamron, Prapai

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Radioactive Iodine for Thyrotoxicosis in Childhood and Adolescence: Treatment and Outcomes von Sirianong, Namwongprom, Kevalee, Unachak, Prapai, Dejkhamron, Supoj, Ua-apisitwong, Molrudee, Ekmahachai

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Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation von Kantaputra, Piranit Nik, Kaewgahya, Massupa, Wiwatwongwana, Atchareeya, Wiwatwongwana, Damrong, Sittiwangkul, Rekwan, Iamaroon, Anak, Dejkhamron, Prapai

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