Nyhan WL - Search Results

1

Two forms of cutis laxa presenting in the newborn period.

Agha A, Sakati NO, Higginbottom MC, Jones KL Jr, Bay C, Nyhan WL. Agha A, et al. Among authors: nyhan wl. Acta Paediatr Scand. 1978 Nov;67(6):775-80. doi: 10.1111/j.1651-2227.1978.tb16260.x. Acta Paediatr Scand. 1978. PMID: 102106

2

Congenital cutis laxa and osteoporosis.

Sakati NO, Nyhan WL. Sakati NO, et al. Among authors: nyhan wl. Am J Dis Child. 1983 May;137(5):452-4. doi: 10.1001/archpedi.1983.02140310034008. Am J Dis Child. 1983. PMID: 6846273

3

Atypical ichthyosiform erythroderma and congenital neurosensory deafness--a distinct syndrome.

Senter TP, Jones KL, Sakati N, Nyhan WL. Senter TP, et al. Among authors: nyhan wl. J Pediatr. 1978 Jan;92(1):68-72. doi: 10.1016/s0022-3476(78)80073-0. J Pediatr. 1978. PMID: 338874

4

A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian.

Higginbottom MC, Sweetman L, Nyhan WL. Higginbottom MC, et al. Among authors: nyhan wl. N Engl J Med. 1978 Aug 17;299(7):317-23. doi: 10.1056/NEJM197808172990701. N Engl J Med. 1978. PMID: 683264

5

A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive defects of the ear, skin, and lower limbs.

Sakati N, Nyhan WL, Tisdale WK. Sakati N, et al. Among authors: nyhan wl. J Pediatr. 1971 Jul;79(1):104-9. doi: 10.1016/s0022-3476(71)80066-5. J Pediatr. 1971. PMID: 4253694 No abstract available.

6

The Börjeson-Forssman-Lehmann syndrome.

Robinson LK, Jones KL, Culler F, Nyhan WL, Sakati N, Jones KL. Robinson LK, et al. Among authors: nyhan wl. Am J Med Genet. 1983 Jul;15(3):457-68. doi: 10.1002/ajmg.1320150311. Am J Med Genet. 1983. PMID: 6683929

7

Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies.

Marsden D, Nyhan WL, Sakati NO. Marsden D, et al. Among authors: nyhan wl. Am J Med Genet. 1994 Sep 1;52(3):334-8. doi: 10.1002/ajmg.1320520316. Am J Med Genet. 1994. PMID: 7810565

8

Joseph's disease: an autosomal dominant neurological disease in the Portuguese of the United States and the Azores Islands.

Rosenberg RN, Nyhan WL, Coutinho P, Bay C. Rosenberg RN, et al. Among authors: nyhan wl. Adv Neurol. 1978;21:33-57. Adv Neurol. 1978. PMID: 735930

9

Autosomal dominant striatonigral degeneration: a clinical, pathological, and biochemical study of a new genetic disorder.

Rosenberg RN, Nyhan WL, Bay C. Rosenberg RN, et al. Among authors: nyhan wl. Trans Am Neurol Assoc. 1976;101:78-80. Trans Am Neurol Assoc. 1976. PMID: 1028273 No abstract available.

10

A syndrome of polydactyly-syndactyly and triphalangeal thumbs in three generations.

Yujnovsky O, Ayala D, Vincitorio A, Viale H, Sakati N, Nyhan WL. Yujnovsky O, et al. Among authors: nyhan wl. Clin Genet. 1974;6(1):51-9. doi: 10.1111/j.1399-0004.1974.tb00630.x. Clin Genet. 1974. PMID: 4372010 No abstract available.

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