S. Srivuthana

发表

Diagnosis and growth hormone (GH) therapy in children with GH deficiency: experience in King Chulalongkorn Memorial Hospital, Thailand.

S. Wacharasindhu, S. Aroonparkmongkol, V. Supornsilchai, 2007, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Kabuki syndrome: report of six Thai children and further phenotypic and genetic delineation.

V. Shotelersuk, S. Wacharasindhu, Rachaneekorn Punyashthiti, 2002, American journal of medical genetics.

Treatment of childhood obesity.

S. Srivuthana, T. Israsena, M. Israngkura, 1980, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Bone mineral density and body composition in prepubertal and adolescent patients with the classical form of 21-hydroxylase deficiency.

Taninee Sahakitrungruang, S. Wacharasindhu, V. Supornsilchai, 2008, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Children with clinical central diabetes insipidus at King Chulalongkorn Memorial Hospital.

S. Srivuthana, Somlak Kittayalaksakun, Wacharasindhu Suttipong, 2005, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele.

K. Suphapeetiporn, V. Shotelersuk, P. Siriwan, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Endocrine Abnormalities in Patients with Frontoethmoidal Encephalomeningocele

S. Srivuthana, S. Wacharasindhu, U. Asawutmangkul, 2005, Hormone Research in Paediatrics.

Disseminated intravascular coagulation. Report of a case in a Thai infant and review of its pathogenesis.

C. Mitrakul, S. Srivuthana, P. Futrakul, 1971, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Distinct craniofacial-skeletal-dermatological dysplasia in a patient with W290C mutation in FGFR2.

S. Lerdlum, V. Shotelersuk, C. Ittiwut, 2002, American journal of medical genetics.

Neonatal screening for hypothyroidism at a university hospital in Thailand.

P. Thaithumyanon, M. Poshyachinda, S. Srivuthana, 1999, The Southeast Asian journal of tropical medicine and public health.

FGFR2 Mutations among Thai Children with Crouzon and Apert Syndromes

V. Shotelersuk, S. Tongkobpetch, C. Ittiwut, 2003, The Journal of craniofacial surgery.

Bone mineral density and body composition in Thai Precocious Puberty girls treated with GnRH agonist.

S. Wacharasindhu, S. Aroonparkmongkol, S. Srivuthana, 2006, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

The clinical presentations of ectopic thyroid gland with results of radioiodine studies.

M. Poshyachinda, S. Srivuthana, T. Israsena, 1977, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Measurement of IGF-1, IGFBP-3 and free IGF-1 levels by ELISA in growth hormone (GH) deficient children before and after GH replacement.

S. Wacharasindhu, S. Aroonparkmongkol, S. Srivuthana, 2002, Asian Pacific journal of allergy and immunology.

Basal luteinizing hormone/follicle stimulating hormone ratio in diagnosis of central precocious puberty.

S. Wacharasindhu, S. Aroonparkmongkol, V. Supornsilchai, 2003, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Establishing gas chromatography-mass spectrometry to diagnose organic acidemias in Thailand.

S. Aroonparkmongkol, S. Jaruratanasirikul, V. Shotelersuk, 2000, The Southeast Asian journal of tropical medicine and public health.

A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene.

A. Theamboonlers, Y. Poovorawan, V. Shotelersuk, 2001, The Southeast Asian journal of tropical medicine and public health.