S. Churesigaew

Children Who Age Rapidly — Progeroid Syndromes

G. M. Martin, R. Ruvalcaba, S. Myhre, 1977, Clinical pediatrics.

A novel mutation of the signal peptide of the preproparathyroid hormone gene associated with autosomal recessive familial isolated hypoparathyroidism.

T. Sunthornthepvarakul, S. Ngowngarmratana, S. Churesigaew, 1999, The Journal of clinical endocrinology and metabolism.

Etiologic study of primary congenital hypothyroidism.

S. Churesigaew, T. Seeherunvong, 1998, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Epilepsy and abnormal calcium metabolism in institutionalized mentally retarded patients.

R. Ruvalcaba, V. Kelley, S. Churesigaew, 1975, American journal of mental deficiency.

Thyrotropin screening for congenital hypothyroidism in Queen Sirikit National Institute of Child Health, Thailand (during year 1995-2000).

Somchit Thaeramanophab, S. Churesigaew, V. Ratrisawasdi, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.