Works by Shotelersuk, Vorasuk

Results: 121

Intronic hexanucleotide repeat expansion in TYMS in monozygotic twins with congenital progressive universal melanosis.

Published in:

Biomedical Reports, 2025, v. 23, n. 2, p. N.PAG, doi. 10.3892/br.2025.2016

By:

Kanchanasutthiyakorn, Sunisa;
Chaiyamahapurk, Sakchai;
Tongkobpetch, Siraprapa;
Santawong, Kanokwan;
Srichomthong, Chalurmpon;
Klomchan, Tippayakarn;
Virochsangaroon, Chaiyaporn;
Pongpanich, Monnat;
Warnnissorn, Prateep;
Pongcharoen, Sutatip;
Shotelersuk, Vorasuk

Publication type:

Article

Tooth agenesis related to a novel KDF1 variant: A case report and literature review.

Published in:

Oral Diseases, 2024, v. 30, n. 8, p. 5195, doi. 10.1111/odi.14930

By:

Intarak, Narin;
Manaspon, Chawan;
Theerapanon, Thanakorn;
Prommanee, Sasiprapa;
Samaranayake, Lakshman;
Shotelersuk, Vorasuk;
Porntaveetus, Thantrira

Publication type:

Article

Authors' reply to: Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG.

Published in:

2024

By:

Sriwattanapong, Kanokwan;
Theerapanon, Thanakorn;
Khamwachirapitak, Chompak;
Sae‐ear, Pannagorn;
Srijunbarl, Anucharte;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Letter to the Editor

Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG.

Published in:

Oral Diseases, 2024, v. 30, n. 2, p. 537, doi. 10.1111/odi.14510

By:

Sriwattanapong, Kanokwan;
Theerapanon, Thanakorn;
Khamwachirapitak, Chompak;
Sae‐ear, Pannagorn;
Srijunbarl, Anucharte;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

PTEN regulates proliferation and osteogenesis of dental pulp cells and adipogenesis of human adipose‑derived stem cells.

Published in:

Oral Diseases, 2023, v. 29, n. 2, p. 735, doi. 10.1111/odi.14030

By:

Nowwarote, Nunthawan;
Osathanon, Thanaphum;
Fournier, Benjamin P.J.;
Theerapanon, Thanakorn;
Yodsanga, Somchai;
Kamolratanakul, Paksinee;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Age‐related dental phenotypes and tooth characteristics of FAM83H‐associated hypocalcified amelogenesis imperfecta.

Published in:

Oral Diseases, 2022, v. 28, n. 3, p. 734, doi. 10.1111/odi.13780

By:

Sriwattanapong, Kanokwan;
Nitayavardhana, Issree;
Theerapanon, Thanakorn;
Thaweesapphithak, Sermporn;
Chantarawaratit, Pintu‐On;
Garuyakich, Rakkierti;
Phokaew, Chureerat;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Tooth ultrastructure of a novel COL1A2 mutation expanding its genotypic and phenotypic spectra.

Published in:

Oral Diseases, 2021, v. 27, n. 5, p. 1257, doi. 10.1111/odi.13657

By:

Intarak, Narin;
Budsamongkol, Thunyaporn;
Theerapanon, Thanakorn;
Chanamuangkon, Theerapat;
Srijunbarl, Anucharte;
Boonprakong, Lawan;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.

Published in:

Oral Diseases, 2018, v. 24, n. 8, p. 1522, doi. 10.1111/odi.12926

By:

Nowwarote, Nunthawan;
Theerapanon, Thanakorn;
Osathanon, Thanaphum;
Pavasant, Prasit;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Genotypic and phenotypic landscapes of 51 pharmacogenes derived from whole-genome sequencing in a Thai population.

Published in:

PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263621

By:

Wankaew, Natnicha;
Chariyavilaskul, Pajaree;
Chamnanphon, Monpat;
Assawapitaksakul, Adjima;
Chetruengchai, Wanna;
Pongpanich, Monnat;
Shotelersuk, Vorasuk

Publication type:

Article

Unraveling the molecular diagnosis of metaphyseal enchondromatosis with D‐2‐hydroxyglutaric aciduria: A 22‐year quest.

Published in:

American Journal of Medical Genetics. Part A, 2024, v. 194, n. 6, p. 1, doi. 10.1002/ajmg.a.63557

By:

Rattanapornsompong, Khanti;
Chetruengchai, Wanna;
Srichomthong, Chalurmpon;
Theerapanon, Thanakorn;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Discrepancy in the degree of polycythemia in a family with a novel nonsense EPOR mutation.

Published in:

2019

By:

Ratarat, Chitsanupong;
Ittiwut, Chupong;
Natesirinilkul, Rungrote;
Sathitsamitpong, Lalita;
Fanhchaksai, Kanda;
Charoenkwan, Pimlak;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Case Study

HLA-B* 1502 screening: Time to clinical practice.

Published in:

2010

By:

Locharernkul, Chaichon;
Shotelersuk, Vorasuk;
Hirankarn, Nattiya

Publication type:

Letter

Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B*1502 allele in Thai population.

Published in:

Epilepsia (Series 4), 2008, v. 49, n. 12, p. 2087, doi. 10.1111/j.1528-1167.2008.01719.x

By:

Locharernkul, Chaichon;
Loplumlert, Jakrin;
Limotai, Chusak;
Korkij, Wiwat;
Desudchit, Tayard;
Tongkobpetch, Siraprapa;
Kangwanshiratada, Oratai;
Hirankarn, Nattiya;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development.

Published in:

PLoS Genetics, 2018, v. 14, n. 11, p. 1, doi. 10.1371/journal.pgen.1007817

By:

Konjikusic, Mia J.;
Yeetong, Patra;
Boswell, Curtis W.;
Lee, Chanjae;
Roberson, Elle C.;
Ittiwut, Rungnapa;
Suphapeetiporn, Kanya;
Ciruna, Brian;
Gurnett, Christina A.;
Wallingford, John B.;
Shotelersuk, Vorasuk;
Gray, Ryan S.

Publication type:

Article

Whole-Exome Sequencing Solved over 2-Decade Kidney Disease Enigma.

Published in:

Nephron, 2021, v. 145, n. 3, p. 311, doi. 10.1159/000514293

By:

Isaranuwatchai, Suramath;
Chanakul, Ankanee;
Ittiwut, Chupong;
Srichomthong, Chalurmpon;
Shotelersuk, Vorasuk;
Praditpornsilpa, Kearkiat;
Suphapeetiporn, Kanya

Publication type:

Article

Functional and pathogenic insights into CNNM4 variants in Jalili syndrome.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-80720-8

By:

Rattanapornsompong, Khanti;
Rinkrathok, Mawika;
Sriwattanapong, Kanokwan;
Shotelersuk, Vorasuk;
Porntaveetus, Thantrira

Publication type:

Article

De novo genome assembly and transcriptome sequencing in foot and mantle tissues of Megaustenia siamensis reveals components of adhesive substances.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-64425-6

By:

Chetruengchai, Wanna;
Jirapatrasilp, Parin;
Srichomthong, Chalurmpon;
Assawapitaksakul, Adjima;
Pholyotha, Arthit;
Tongkerd, Piyoros;
Shotelersuk, Vorasuk;
Panha, Somsak

Publication type:

Article

A novel BAG5 variant impairs the ER stress response pathway, causing dilated cardiomyopathy and arrhythmia.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-62764-y

By:

Wongong, Rutairat;
Kijtawornrat, Anusak;
Srichomthong, Chalurmpon;
Tongkobpeth, Siraprapa;
Od-Ek, Phichittra;
Assawapitaksakul, Adjima;
Caengprasath, Natarin;
Khongphatthanayothin, Apichai;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Comprehensive genome assembly reveals genetic diversity and carcass consumption insights in critically endangered Asian king vultures.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-59990-9

By:

Buthasane, Wannapol;
Shotelersuk, Vorasuk;
Chetruengchai, Wanna;
Srichomthong, Chalurmpon;
Assawapitaksakul, Adjima;
Tangphatsornruang, Sithichoke;
Pootakham, Wirulda;
Sonthirod, Chutima;
Tongsima, Sissades;
Wangkumhang, Pongsakorn;
Wilantho, Alisa;
Thongphakdee, Ampika;
Sanannu, Saowaphang;
Poksawat, Chaianan;
Nipanunt, Tarasak;
Kasorndorkbua, Chaiyan;
Koepfli, Klaus-Peter;
Pukazhenthi, Budhan S.;
Suriyaphol, Prapat;
Wongsurawat, Thidathip

Publication type:

Article

Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists.

Published in:

Clinical & Molecular Hepatology, 2019, v. 25, n. 4, p. 412, doi. 10.3350/cmh.2018.0114

By:

Phowthongkum, Prasit;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

ZRS 406A>G mutation in patients with tibial hypoplasia, Polydactyly and triphalangeal first fingers.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 8, p. 467, doi. 10.1038/jhg.2014.50

By:

Norbnop, Phatchara;
Srichomthong, Chalurmpon;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

A common and two novel GBA mutations in Thai patients with Gaucher disease.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 9, p. 594, doi. 10.1038/jhg.2013.60

By:

Tammachote, Rachaneekorn;
Tongkobpetch, Siraprapa;
Srichomthong, Chalurmpon;
Phipatthanananti, Kampon;
Pungkanon, Suthipong;
Wattanasirichaigoon, Duangrurdee;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Novel CNNM4 variant and clinical features of Jalili syndrome.

Published in:

Clinical Genetics, 2023, v. 103, n. 2, p. 256, doi. 10.1111/cge.14258

By:

Rattanapornsompong, Khanti;
Gavila, Patcharaporn;
Tungsanga, Somkanya;
Chanakul, Ankanee;
Apivatthakakul, Atitaya;
Tengsujaritkul, Maliwan;
Tongsong, Theera;
Theerapanon, Thanakorn;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

Novel BMP1, CRTAP, and SERPINF1 variants causing autosomal recessive osteogenesis imperfecta.

Published in:

Clinical Genetics, 2022, v. 102, n. 3, p. 242, doi. 10.1111/cge.14172

By:

Kuptanon, Chulaluck;
Thamkunanon, Verasak;
Srichomthong, Chalurmpon;
Theerapanon, Thanakorn;
Suphapeetiporn, Kanya;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

The Thai reference exome (T‐REx) variant database.

Published in:

Clinical Genetics, 2021, v. 100, n. 6, p. 703, doi. 10.1111/cge.14060

By:

Shotelersuk, Vorasuk;
Wichadakul, Duangdao;
Ngamphiw, Chumpol;
Srichomthong, Chalurmpon;
Phokaew, Chureerat;
Wilantho, Alisa;
Pakchuen, Sujiraporn;
Nakhonsri, Vorthunju;
Shaw, Philip James;
Wasitthankasem, Rujipat;
Piriyapongsa, Jittima;
Wangkumhang, Pongsakorn;
Assawapitaksakul, Adjima;
Chetruengchai, Wanna;
Lapphra, Keswadee;
Khuninthong, Athiphat;
Makarawate, Pattarapong;
Suphapeetiporn, Kanya;
Mahasirimongkol, Surakameth;
Satproedprai, Nusara

Publication type:

Article

Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand.

Published in:

Clinical Genetics, 2021, v. 100, n. 1, p. 100, doi. 10.1111/cge.13963

By:

Kamolvisit, Wuttichart;
Phowthongkum, Prasit;
Boonsimma, Ponghatai;
Kuptanon, Chulaluck;
Rojnueangnit, Kitiwan;
Wattanasirichaigoon, Duangrurdee;
Chanvanichtrakool, Mongkol;
Phuaksaman, Chutima;
Wiromrat, Pattara;
Srichomthong, Chalurmpon;
Ittiwut, Chupong;
Phokaew, Chureerat;
Ittiwut, Rungnapa;
Assawapitaksakul, Adjima;
Chetruengchai, Wanna;
Buasong, Aayalida;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 2, p. 225, doi. 10.1038/ejhg.2012.133

By:

Yeetong, Patra;
Ausavarat, Surasawadee;
Bhidayasiri, Roongroj;
Piravej, Krisna;
Pasutharnchat, Nath;
Desudchit, Tayard;
Chunharas, Chaipat;
Loplumlert, Jakrin;
Limotai, Chusak;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

PDGFRa mutations in humans with isolated cleft palate.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 10, p. 1058, doi. 10.1038/ejhg.2012.55

By:

Rattanasopha, Sawitree;
Tongkobpetch, Siraprapa;
Srichomthong, Chalurmpon;
Siriwan, Pichit;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

A Frameshift Mutation in PEN-2 Causes Familial Comedones Syndrome.

Published in:

Dermatology (10188665), 2015, v. 231, n. 1, p. 77, doi. 10.1159/000382122

By:

Panmontha, Wipa;
Rerknimitr, Pawinee;
Yeetong, Patra;
Srichomthong, Chalurmpon;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Expanding Phenotypic Spectrum of Familial Comedones.

Published in:

Dermatology (10188665), 2014, v. 228, n. 3, p. 215, doi. 10.1159/000358170

By:

Rerknimitr, Pawinee;
Korkij, Wiwat;
Wititsuwannakul, Jade;
Panmontha, Wipa;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Expanding phenotypic spectrum of familial comedones.

Published in:

2014

By:

Rerknimitr, Pawinee;
Korkij, Wiwat;
Wititsuwannakul, Jade;
Panmontha, Wipa;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Journal Article

Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia Congenita.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 1, p. 171, doi. 10.1210/js.2018-00270

By:

Suthiworachai, Chanisara;
Tammachote, Rachaneekorn;
Srichomthong, Chalurmpon;
Ittiwut, Rungnapa;
Suphapeetiporn, Kanya;
Sahakitrungruang, Taninee;
Shotelersuk, Vorasuk

Publication type:

Article

Pre-implantation genetic testing for Marfan syndrome using mini-sequencing.

Published in:

Journal of Obstetrics & Gynaecology, 2022, v. 42, n. 7, p. 2846, doi. 10.1080/01443615.2022.2109957

By:

Piyamongkol, Sirivipa;
Makonkawkeyoon, Krit;
Shotelersuk, Vorasuk;
Sreshthaputra, Opas;
Pantasri, Tawiwan;
Sittiwangkul, Rekwan;
Tongsong, Theera;
Piyamongkol, Wirawit

Publication type:

Article

Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-29924-y

By:

Chokvithaya, Suphalak;
Caengprasath, Natarin;
Buasong, Aayalida;
Jantasuwan, Supavadee;
Santawong, Kanokwan;
Leela-adisorn, Netchanok;
Tongkobpetch, Siraprapa;
Ittiwut, Chupong;
Saengow, Vitchayaporn Emarach;
Kamolvisit, Wuttichart;
Boonsimma, Ponghatai;
Bongsebandhu-phubhakdi, Saknan;
Shotelersuk, Vorasuk

Publication type:

Article

Utilisation of exome sequencing for muscular disorders in Thai paediatric patients: diagnostic yield and mutational spectrum.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28405-6

By:

Summa, Sarinya;
Ittiwut, Chupong;
Kulsirichawaroj, Pimchanok;
Paprad, Tanitnun;
Likasitwattanakul, Surachai;
Sanmaneechai, Oranee;
Boonsimma, Ponghatai;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-26291-y

By:

Isaranuwatchai, Suramath;
Chanakul, Ankanee;
Ittiwut, Chupong;
Ittiwut, Rungnapa;
Srichomthong, Chalurmpon;
Shotelersuk, Vorasuk;
Suphapeetiporn, Kanya;
Praditpornsilpa, Kearkiat

Publication type:

Article

Comparative transcriptome profiles of human dental pulp stem cells from maxillary and mandibular teeth.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12867-1

By:

Faruangsaeng, Thira;
Thaweesapphitak, Sermporn;
Khamwachirapitak, Chompak;
Porntaveetus, Thantrira;
Shotelersuk, Vorasuk

Publication type:

Article

A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-19334-x

By:

Sinthuwiwat, Thivaratana;
Buranapraditkun, Supranee;
Kamolvisit, Wuttichart;
Tongkobpetch, Siraprapa;
Chetruengchai, Wanna;
Srichomthong, Chalurmpon;
Assawapitaksakul, Adjima;
Phokaew, Chureerat;
Kueanjinda, Patipark;
Palaga, Tanapat;
Boonpiyathad, Tadech;
Suphapeetiporn, Kanya;
Hirankarn, Nattiya;
Shotelersuk, Vorasuk

Publication type:

Article

Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene.

Published in:

Clinical Endocrinology, 2009, v. 70, n. 4, p. 623, doi. 10.1111/j.1365-2265.2008.03367.x

By:

Supornsilchai, Vichit;
Sahakitrungruang, Taninee;
Wongjitrat, Nattakarn;
Wacharasindhu, Suttipong;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome.

Published in:

Hormone Research in Paediatrics, 2019, v. 92, n. 3, p. 196, doi. 10.1159/000501169

By:

Dejkhamron, Prapai;
Ittiwut, Chupong;
TangNgam, Hataitip;
Sunkonkit, Kanokkarn;
Natesirinilkul, Rungrote;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Functional Characterization of Vasopressin Receptor 2 Mutations Causing Partial and Complete Congenital Nephrogenic Diabetes Insipidus in Thai Families.

Published in:

Hormone Research in Paediatrics, 2010, v. 73, n. 5, p. 349, doi. 10.1159/000308167

By:

Sahakitrungruang, Taninee;
Tee, Meng Kian;
Rattanachartnarong, Natthakorn;
Shotelersuk, Vorasuk;
Suphapeetiporn, Kanya;
Miller, Walter L.

Publication type:

Article

Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-023-01771-w

By:

Chetruengchai, Wanna;
Phowthongkum, Prasit;
Shotelersuk, Vorasuk

Publication type:

Article

In vitro Correction of a Novel Splicing Alteration in the BTK Gene by Using Antisense Morpholino Oligonucleotides.

Published in:

Archivum Immunologiae & Therapiae Experimentalis, 2014, v. 62, n. 5, p. 431, doi. 10.1007/s00005-014-0283-0

By:

Rattanachartnarong, Natthakorn;
Tongkobpetch, Siraprapa;
Chatchatee, Pantipa;
Daengsuwan, Tassalapa;
Ittiwut, Chupong;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Novel CTSK mutation resulting in an entire exon 2 skipping in a Thai girl with pycnodysostosis.

Published in:

Pediatrics International, 2013, v. 55, n. 5, p. 651, doi. 10.1111/ped.12091

By:

Utokpat, Pattarapa;
Panmontha, Wipa;
Tongkobpetch, Siraprapa;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.887121

By:

Ashouri, Saeideh;
Khor, Seik-Soon;
Hitomi, Yuki;
Sawai, Hiromi;
Nishida, Nao;
Sugiyama, Masaya;
Kawai, Yosuke;
Posuwan, Nawarat;
Tangkijvanich, Pisit;
Komolmit, Piyawat;
Tsuiji, Makoto;
Shotelersuk, Vorasuk;
Poovorawan, Yong;
Mizokami, Masashi;
Tokunaga, Katsushi

Publication type:

Article

Nagashima-Type Palmoplantar Keratosis with Compound Heterozygous Mutations in SERPINB7.

Published in:

Case Reports in Dermatology, 2020, v. 12, n. 3, p. 241, doi. 10.1159/000509535

By:

Songsantiphap, Chankiat;
Suwanwatana, Jirat;
Ittiwut, Chupong;
Asawanonda, Pravit;
Rerknimitr, Pawinee;
Shotelersuk, Vorasuk

Publication type:

Article

Mutation analysis and prenatal diagnosis of a family with Griscelli syndrome type 2: two novel mutations in the RAB27A gene.

Published in:

2017

By:

Yeetong, Patra;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Letter

Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene.

Published in:

Endocrine (1355008X), 2011, v. 40, n. 1, p. 62, doi. 10.1007/s12020-011-9450-9

By:

Supornsilchai, Vichit;
Hiranras, Yodporn;
Wacharasindhu, Suttipong;
Mahayosnond, Atchara;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

Article

Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy.

Published in:

Endocrine (1355008X), 2010, v. 37, n. 2, p. 261, doi. 10.1007/s12020-009-9292-x

By:

Snabboon, Thiti;
Plengpanich, Wanee;
Houngngam, Natnicha;
Buranasupkajorn, Patinut;
Plengvidhya, Nattachet;
Sereepapong, Wisan;
Sunthornyothin, Sarat;
Shotelersuk, Vorasuk

Publication type:

Article

Identification of two novel aquaporin-2 mutations in a Thai girl with congenital nephrogenic diabetes insipidus.

Published in:

Endocrine (1355008X), 2008, v. 33, n. 2, p. 210

By:

Taninee Sahakitrungruang;
Suttipong Wacharasindhu;
Thivaratana Sinthuwiwat;
Vichit Supornsilchai;
Kanya Suphapeetiporn;
Vorasuk Shotelersuk

Publication type:

Article