Woolf LI - Search Results

1

The dietary treatment of inborn errors of metabolism.

Woolf LI. Woolf LI. Proc Nutr Soc. 1976 May;35(1):31-6. Proc Nutr Soc. 1976. PMID: 781683 Review. No abstract available.

2

Recent studies on galactosaemia, phenylketonuria and homocystinuria.

Woolf LI. Woolf LI. Proc Nutr Soc. 1968 Mar;27(1):88-95. doi: 10.1079/pns19680019. Proc Nutr Soc. 1968. PMID: 4880444 Review. No abstract available.

3

Nutrition in relation to phenylketonuria.

WOOLF LI. WOOLF LI. Proc Nutr Soc. 1962;21:21-9. doi: 10.1079/pns19620006. Proc Nutr Soc. 1962. PMID: 14008283 No abstract available.

4

Tyrosinosis (inborn hepato-renal dysfunction).

Woolf LI. Woolf LI. Proc R Soc Med. 1966 Sep;59(9):814-5. doi: 10.1177/003591576605900903. Proc R Soc Med. 1966. PMID: 5921563 Free PMC article. No abstract available.

5

Recent work on phenylketonuria and maple syrup urine disease (leucinosis).

WOOLF LI. WOOLF LI. Proc R Soc Med. 1962 Oct;55(10):824-6. doi: 10.1177/003591576205501001. Proc R Soc Med. 1962. PMID: 14001839 Free PMC article. No abstract available.

6

The dietary treatment of phenylketonuria.

WOOLF LI, GRIFFITHS R, MONCRIEFF A, COATES S, DILLISTONE F. WOOLF LI, et al. Arch Dis Child. 1958 Feb;33(167):31-45. doi: 10.1136/adc.33.167.31. Arch Dis Child. 1958. PMID: 13509741 Free PMC article. No abstract available.

7

The dietary treatment of phenylketonuria: not proven.

Woolf LI. Woolf LI. Dev Med Child Neurol. 1967 Apr;9(2):244-5. doi: 10.1111/j.1469-8749.1967.tb02254.x. Dev Med Child Neurol. 1967. PMID: 6059329 No abstract available.

8

INHERITED METABOLIC DISORDERS: ERRORS OF PHENYLALANINE AND TYROSINE METABOLISM.

WOOLF LI. WOOLF LI. Adv Clin Chem. 1963;6:97-230. doi: 10.1016/s0065-2423(08)60239-5. Adv Clin Chem. 1963. PMID: 14281820 Review. No abstract available.

9

Paediatric screening for genetically determined metabolic diseases.

Woolf LI. Woolf LI. Proc R Soc Med. 1968 Aug;61(8):766-7. doi: 10.1177/003591576806100811. Proc R Soc Med. 1968. PMID: 5673397 Free PMC article. No abstract available.

10

Iminoglycinuria--a "harmless" inborn error of metabolism?

Fraser GR, Friedmann AI, Patton VM, Wade DN, Woolf LI. Fraser GR, et al. Among authors: woolf li. Humangenetik. 1968;6(4):362-7. doi: 10.1007/BF00286806. Humangenetik. 1968. PMID: 5713621 No abstract available.

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