Hasil Pencarian - Objoon Trachoo

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  1. 1
    Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features

    Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features oleh Sira Korpaisarn, Objoon Trachoo, Chutintorn Sriphrapradang

    Diterbitkan 2013-01-01
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  2. 2
    A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease

    A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease oleh Sira Korpaisarn, Objoon Trachoo, Bhakbhoom Panthan, Rangsima Aroonroch, Ronnarat Suvikapakornkul, Chutintorn Sriphrapradang

    Diterbitkan 2017-08-01
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  3. 3
    Successful Treatment of Schwartz-Jampel Syndrome with Botulinum Toxin Type A

    Successful Treatment of Schwartz-Jampel Syndrome with Botulinum Toxin Type A oleh Panittra Suphatsathienkul, Kullasate Sakpichaisakul, Thanin Wechapinan, Objoon Trachoo, Sorawit Virawan, Rungsima Wanitphakdeedecha

    Diterbitkan 2024-01-01
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  4. 4
    Fine-Needle Aspiration Cytology of Parathyroid Carcinoma Mimic Hürthle Cell Thyroid Neoplasm

    Fine-Needle Aspiration Cytology of Parathyroid Carcinoma Mimic Hürthle Cell Thyroid Neoplasm oleh Chutintorn Sriphrapradang, Pattana Sornmayura, Niramol Chanplakorn, Objoon Trachoo, Pattarana Sae-Chew, Rangsima Aroonroch

    Diterbitkan 2014-01-01
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  5. 5
    Epileptic spasms related to neuronal differentiation factor 2 (NEUROD2) mutation respond to combined vigabatrin and high dose prednisolone therapy

    Epileptic spasms related to neuronal differentiation factor 2 (NEUROD2) mutation respond to combined vigabatrin and high dose prednisolone therapy oleh Kullasate Sakpichaisakul, Rachata Boonkrongsak, Punjama Lertbutsayanukul, Nareenart Iemwimangsa, Sommon Klumsathian, Bhakbhoom Panthan, Objoon Trachoo

    Diterbitkan 2022-12-01
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  6. 6
    Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single center.

    Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single ce... oleh Chonthicha Satirapod, Matchuporn Sukprasert, Bhakbhoom Panthan, Angkana Charoenyingwattana, Pawares Chitayanan, Wasun Chantratita, Wicharn Choktanasiri, Objoon Trachoo, Suradej Hongeng

    Diterbitkan 2019-01-01
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  7. 7
    Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service.

    Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service. oleh Objoon Trachoo, Teerapat Yingchoncharoen, Tawai Ngernsritrakul, Nareenart Iemwimangsa, Bhakbhoom Panthan, Sommon Klumsathian, Sasima Srisukh, Anucha Mukdadilok, Sithakom Phusanti, Angkana Charoenyingwattana, Takol Chareonsirisuthigul, Wasun Chantratita, Tarinee Tangcharoen

    Diterbitkan 2022-01-01
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  8. 8
    Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service

    Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service oleh Objoon Trachoo, Teerapat Yingchoncharoen, Tawai Ngernsritrakul, Nareenart Iemwimangsa, Bhakbhoom Panthan, Sommon Klumsathian, Sasima Srisukh, Anucha Mukdadilok, Sithakom Phusanti, Angkana Charoenyingwattana, Takol Chareonsirisuthigul, Wasun Chantratita, Tarinee Tangcharoen

    Diterbitkan 2022-01-01
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