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Kantaputra P.N.
หน่วยงาน มหาวิทยาลัยเชียงใหม่
และรู้จักในชื่อของ
- Kantoputra P.N.
- Kantaputra PN.
จำนวนงานวิจัยจำแนกรายปี
บุคคลที่เคยร่วมงานวิจัย
ความเชี่ยวชาญ
ไม่มีข้อมูลความเชี่ยวชาญ
บุคคลที่เคยร่วมงานวิจัย
# นักวิจัย ร่วมงาน
1 Kayserili H. 5
2 Kaewgahya M. 5
3 Dejkhamron P. 4
4 Iamaroon A. 4
5 Guven Y. 4
6 Visrutaratna P. 4
7 Sittiwangkul R. 4
8 Chalidapong P. 3
9 Unachak K. 3
10 Sripathomsawat W. 3
11 Praphanphoj V. 3
12 Niikawa N. 3
13 Lapunzina P. 2
14 Thongboonkerd V. 2
15 Tenorio J. 2
16 Romanelli V. 2
17 Sonsuwan N. 2
18 Uttarilli A. 2
19 Kantaputra W. 2
20 Ohazama A. 2
21 Wiwatwongwana A. 2
22 Patikulsila P. 2
23 Wiwatwongwana D. 2
24 Aktoren O. 2
25 Dalal A. 2
26 Sutthimethakorn S. 2
27 Khemaleelakul U. 2
28 Balci M.C. 2
29 Malikaew P. 2
30 Chiewcharnvalijkit M.S.K. 2
31 Wairatpanich K. 2
32 Mevate U. 2
33 Matin T. 2
34 Kunachaichote J. 2
35 Eiumtrakul P. 2
36 Aramrattana A. 2
37 Opastirakul S. 2
38 Pongprot Y. 2
39 Pho-iam T. 2
40 Mundlos S. 2
41 Tochareontanaphol C. 2
42 Schutte B.C. 2
43 Sumitsawan Y. 2
44 Mongkolchaisup S. 1
45 Matangkasombut O. 1
46 Hamada T. 1
47 Stanier P. 1
48 Kumchai T. 1
49 McGrath J.A. 1
50 Moore G.E. 1
51 Gorlin RJ. 1
52 Hoshino A. 1
53 Lees M. 1
54 McEntagart M. 1
55 Masrour N. 1
56 Pauws E. 1
57 Altunoglu U. 1
58 Kaewkahya M. 1
59 Uyguner Z.O. 1
60 Bongkochwilawan C. 1
61 Erdem A.P. 1
62 Kaewkhampa A. 1
63 Tananuvat N. 1
64 Sangruchi T. 1
65 Sudasna J. 1
66 Pruksachatkunakorn C. 1
67 Vanittanakom P. 1
68 van den Ouweland A. 1
69 Ukarapol N. 1
70 Ishida T. 1
71 Shears D.J. 1
72 Kwee M.L. 1
73 Sugawara H. 1
74 Harada N. 1
75 Matsumoto N. 1
76 Isidor B. 1
77 Hennig B.P. 1
78 Koolvisoot A. 1
79 Hall J.G. 1
80 Ausawamongkolkul A. 1
81 Tayavitit S. 1
82 Klopocki E. 1
83 Ohashi H. 1
84 Sato M. 1
85 Vieira A.R. 1
86 Malaivijitnond S. 1
87 Heering J. 1
88 Dotsch V. 1
89 Khankasikum T. 1
90 Praditsup O. 1
91 Kinoshita A. 1
92 Ogino T. 1
93 Tomita H. 1
94 Ohta T. 1
95 Fukushima Y. 1
96 Paramee M. 1
ปี
# พ.ศ. จำนวน
1 2557 10
2 2556 2
3 2555 3
4 2554 2
5 2553 2
6 2550 2
7 2549 1
8 2548 3
9 2547 4
10 2546 3
11 2545 6
12 2544 9
13 2543 1
14 2542 2
15 2541 1
ผลงานวิจัย
# หัวเรื่อง
ปี พ.ศ. 2557
1 BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells
2 Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations
3 Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation
4 Enamel-renal-gingival syndrome and FAM20A mutations
5 Enamel-renal-gingival syndrome and FAM20A mutations
6 Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI
7 Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation
8 Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation
9 Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation
10 Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation
ปี พ.ศ. 2556
11 A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
12 A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
ปี พ.ศ. 2555
13 Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation
14 Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient
15 Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
ปี พ.ศ. 2554
16 Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate
17 Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations
ปี พ.ศ. 2553
18 A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
19 Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q
ปี พ.ศ. 2550
20 Children's attitudes toward behavior management techniques used by dentists
21 Children's attitudes toward behavior management techniques used by dentists
ปี พ.ศ. 2549
22 A newly recognized polyosteolysis/hyperostosis syndrome
ปี พ.ศ. 2548
23 A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?
24 Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters)
25 A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?
ปี พ.ศ. 2547
26 Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome
27 Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al.
28 Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome
29 Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al
ปี พ.ศ. 2546
30 Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia
31 A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5
32 A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5
ปี พ.ศ. 2545
33 Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family
34 A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: A new distal symphalangism syndrome?
35 Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family
36 A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet
37 A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai family
38 Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings
ปี พ.ศ. 2544
39 Digitotalar dysmorphism with craniofacial and other new associated abnormalities
40 Laurin-Sandrow syndrome with additional associated manifestations
41 Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome
42 Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome?
43 A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth
44 Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome
45 Dentinogenesis imperfecta-associated syndromes
46 Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome?
47 Digitotalar dysmorphism with craniofacial and other new associated abnormalities
ปี พ.ศ. 2543
48 Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family
ปี พ.ศ. 2542
49 Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome
50 Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type
ปี พ.ศ. 2541
51 Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings