phenylalanine and Incontinentia Pigmenti Achromians

phenylalanine has been researched along with Incontinentia Pigmenti Achromians in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	8 (80.00)	18.7374
1990's	1 (10.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (10.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ben Dridi, MF; Dhondt, JL; El Asmi, M; Feki, M; Jemaa, R; Kaabachi, N; Khemir, S; Mebazaa, A; Sanhaji, H; Tebib, N	1
BAN, TA; LEHMANN, HE	1
Klein, LE; Nordlund, JJ	1
Bechelli, LM; Gonçalves, RP; Pagnano, PM; Tanaka, AM	1
Mishima, Y	1
Butler, MG	1
Edmund, J; Egeberg, J; Jensen, OA	1
Tronnier, H	1
Giunti, A	1
Bamshad, J	1

Reviews

1 review(s) available for phenylalanine and Incontinentia Pigmenti Achromians

Article	Year
A post melanosomal era: control of melanogenesis and melanoma growth. Pigment cell research, 1992, Volume: Suppl 2 Topics: Adolescent; Animals; Boron; Boron Compounds; Cricetinae; Fatty Acids, Unsaturated; Gene Expression Regulation, Neoplastic; Hair Color; Humans; Infant, Newborn; Isotopes; Male; Melanins; Melanocytes; Melanoma; Melanoma, Experimental; Models, Biological; Monophenol Monooxygenase; Neoplasm Proteins; Neutrons; Phenylalanine; Pigmentation Disorders; Protein Processing, Post-Translational; Pyrones; Radiation-Sensitizing Agents; Skin Pigmentation; Subcellular Fractions; Swine	1992

Article

Year

A post melanosomal era: control of melanogenesis and melanoma growth.

Pigment cell research, 1992, Volume: Suppl 2

Topics: Adolescent; Animals; Boron; Boron Compounds; Cricetinae; Fatty Acids, Unsaturated; Gene Expression Regulation, Neoplastic; Hair Color; Humans; Infant, Newborn; Isotopes; Male; Melanins; Melanocytes; Melanoma; Melanoma, Experimental; Models, Biological; Monophenol Monooxygenase; Neoplasm Proteins; Neutrons; Phenylalanine; Pigmentation Disorders; Protein Processing, Post-Translational; Pyrones; Radiation-Sensitizing Agents; Skin Pigmentation; Subcellular Fractions; Swine

1992

Other Studies

9 other study(ies) available for phenylalanine and Incontinentia Pigmenti Achromians

Article	Year
Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment. Clinical neurology and neurosurgery, 2011, Volume: 113, Issue:9 Topics: Age of Onset; Amino Acids; Child, Preschool; Developmental Disabilities; Female; Gas Chromatography-Mass Spectrometry; Health Services Accessibility; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Neonatal Screening; Phenylalanine; Phenylketonurias; Pigmentation Disorders; Retrospective Studies; Speech Disorders; Tunisia	2011
SKIN PIGMENTATION, A RARE SIDE EFFECT OF CHLORPROMAZINE. Canadian Psychiatric Association journal, 1965, Volume: 10 Topics: Chemical Phenomena; Chemistry; Chlorpromazine; Diagnosis, Differential; Drug Therapy; Epilepsy; Eye Manifestations; Intellectual Disability; Melanins; Melanosis; Pathology; Perphenazine; Phenobarbital; Phenylalanine; Photosensitivity Disorders; Pigmentation Disorders; Prochlorperazine; Schizophrenia; Skin Pigmentation; Toxicology	1965
Genetic basis of pigmentation and its disorders. International journal of dermatology, 1981, Volume: 20, Issue:10 Topics: Albinism; Animals; Cell Differentiation; Color; Humans; Lentigo; Melanins; Melanocytes; Melanoma; Mice; Monophenol Monooxygenase; Nevus; Phenylalanine; Pigmentation; Pigmentation Disorders; Skin; Syndrome; Tyrosine	1981
[Cutaneous dyschromia in three cases of phenylketonuria. Quantitative ultrastructural study of the basal layer of the epidermis (author's transl)]. Annales de dermatologie et de venereologie, 1978, Volume: 105, Issue:2 Topics: Child; Epidermis; Erythema; Female; Hair Color; Humans; Keratins; Male; Melanins; Phenylalanine; Phenylketonurias; Pigmentation Disorders; Tyrosine	1978
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome. American journal of human genetics, 1989, Volume: 45, Issue:1 Topics: Adolescent; Adult; Catecholamines; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 15; Eye Color; Female; Hair Color; Humans; Infant; Male; Melanocyte-Stimulating Hormones; Phenylalanine; Pigmentation Disorders; Prader-Willi Syndrome; Skin; Tyrosine	1989
The effect of a phenylalanine-tyrosine low diet on the growth and morphology of transplantable malignant melanomas of the Syrian golden hamster (Mesocricetus auratus). Acta pathologica et microbiologica Scandinavica. Section A, Pathology, 1973, Volume: 81, Issue:4 Topics: Animals; Cell Transformation, Neoplastic; Copper; Cricetinae; Diet; Hair; Melanins; Melanocytes; Melanoma; Microscopy, Electron; Neoplasm Metastasis; Neoplasm Transplantation; Neoplasms, Experimental; Phenylalanine; Pigmentation Disorders; Protein Deficiency; Skin; Skin Neoplasms; Transplantation, Homologous; Tyrosine	1973
[Diagnosis and therapy of the secondary disease: dermatology]. International journal of clinical pharmacology, therapy and toxicology, 1973, Volume: 8, Issue:4 Topics: Candidiasis; Diabetes Complications; Female; Herpes Zoster; Humans; Liver Diseases; Malabsorption Syndromes; Male; Parathyroid Diseases; Phenylalanine; Pigmentation Disorders; Skin Diseases; Skin Manifestations; Tryptophan; Tyrosine; Vitamin B 12 Deficiency	1973
[Ochronotic arthropathy]. La Chirurgia degli organi di movimento, 1969, Volume: 58, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Joint Diseases; Male; Middle Aged; Ochronosis; Phenylalanine; Pigmentation Disorders; Radiography; Tyrosine	1969
Cutaneous manifestations of disorders of metabolism of phenylalanine-tyrosine. Missouri medicine, 1971, Volume: 68, Issue:6 Topics: Albinism; Amino Acid Metabolism, Inborn Errors; Humans; Phenylalanine; Pigmentation Disorders; Skin Manifestations; Tyrosine	1971