عوز السلفاتاز المتعدد (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "عوز السلفاتاز المتعدد" in Arabic language version.

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13nih.gov

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archive.org

Burk, R؛ Valle، D؛ Thomas، GH؛ Miller، C؛ Moser، A؛ Moser، H؛ Rosenbaum، KN (1984). "Early manifestations of multiple sulfatase deficiency†". The Journal of Pediatrics. ج. 104 ع. 4: 574–8. DOI:10.1016/S0022-3476(84)80550-8. PMID:6142938.

doi.org

Dierks, T؛ Schmidt, B؛ Borissenko, Lv؛ Peng, J؛ Preusser, A؛ Mariappan, M؛ Von, Figura K (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.
Schmidt, B؛ Selmer, T؛ Ingendoh, A؛ Von, Figura K (يوليو 1995). "A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency". Cell. ج. 82 ع. 2: 271–8. DOI:10.1016/0092-8674(95)90314-3. PMID:7628016. S2CID:5864312.
Soong BW، Casamassima AC، Fink JK، Constantopoulos G، Horwitz AL (1988). "Multiple sulfatase deficiency". Neurology. ج. 38 ع. 8: 1273–5. DOI:10.1212/wnl.38.8.1273. PMID:2899861. S2CID:35222500.
Burk, R؛ Valle، D؛ Thomas، GH؛ Miller، C؛ Moser، A؛ Moser، H؛ Rosenbaum، KN (1984). "Early manifestations of multiple sulfatase deficiency†". The Journal of Pediatrics. ج. 104 ع. 4: 574–8. DOI:10.1016/S0022-3476(84)80550-8. PMID:6142938.
Farooqui AA، Horrocks LA (1984). "Biochemical aspects of globoid and metachromatic leukodystrophies". Neurochem Pathol. ج. 2 ع. 3: 189–218. DOI:10.1007/BF02834352. PMID:6152665. S2CID:36099212. مؤرشف من الأصل في 2021-09-05.
Cosma MP، Pepe S، Annunziata I (مايو 2003). "The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases". Cell. ج. 113 ع. 4: 445–56. DOI:10.1016/S0092-8674(03)00348-9. PMID:12757706. S2CID:15095377.
Annunziata I، Bouchè V، Lombardi A (سبتمبر 2007). "Multiple sulfatase deficiency is due to hypomorphic mutations of the SUMF1 gene". Human Mutation. ج. 28 ع. 9: 298. DOI:10.1002/humu.9504. PMID:17657823. S2CID:8500605.
Dierks T، Schmidt B، Borissenko LV (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.
Preusser-Kunze A، Mariappan M، Schmidt B، Gande SL، Mutenda K، Wenzel D، von Figura K، Dierks T (أبريل 2005). "Molecular Characterization of the Human C(alpha)-formylglycine-generating Enzyme". Journal of Biological Chemistry. ج. 280 ع. 15: 14900–14910. DOI:10.1074/jbc.M413383200. PMID:15657036.
Landgrebe J، Dierks T، Schmidt B (أكتوبر 2003). "The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes". Gene. ج. 316: 47–56. DOI:10.1016/S0378-1119(03)00746-7. PMID:14563551. مؤرشف من الأصل في 2022-03-03.
Schlotawa، L؛ Adang، LA؛ Radhakrishnan، K؛ Ahrens-Nicklas، RC (13 مايو 2020). "Multiple sulfatase deficiency: A disease comprising mucopolysaccharidosis, sphingolipidosis, and more caused by a defect in posttranslational modification". International Journal of Molecular Sciences. ج. 21 ع. 10: 3448. DOI:10.3390/ijms21103448. PMC:7279497. PMID:32414121.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dierks, T؛ Schmidt, B؛ Borissenko, Lv؛ Peng, J؛ Preusser, A؛ Mariappan, M؛ Von, Figura K (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.
Schmidt, B؛ Selmer, T؛ Ingendoh, A؛ Von, Figura K (يوليو 1995). "A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency". Cell. ج. 82 ع. 2: 271–8. DOI:10.1016/0092-8674(95)90314-3. PMID:7628016. S2CID:5864312.
Soong BW، Casamassima AC، Fink JK، Constantopoulos G، Horwitz AL (1988). "Multiple sulfatase deficiency". Neurology. ج. 38 ع. 8: 1273–5. DOI:10.1212/wnl.38.8.1273. PMID:2899861. S2CID:35222500.
Burk, R؛ Valle، D؛ Thomas، GH؛ Miller، C؛ Moser، A؛ Moser، H؛ Rosenbaum، KN (1984). "Early manifestations of multiple sulfatase deficiency†". The Journal of Pediatrics. ج. 104 ع. 4: 574–8. DOI:10.1016/S0022-3476(84)80550-8. PMID:6142938.
Schlotawa، L؛ Adang، L؛ De Castro، M؛ Ahrens-Nicklas، R (2019). "Multiple sulfatase deficiency". في Adam، MP؛ Ardinger، HH؛ Pagon، RA؛ Wallace، SE؛ Bean، LJH؛ Mirzaa، G؛ Amemiya، A (المحررون). GeneReviews. PMID:30896912.
Farooqui AA، Horrocks LA (1984). "Biochemical aspects of globoid and metachromatic leukodystrophies". Neurochem Pathol. ج. 2 ع. 3: 189–218. DOI:10.1007/BF02834352. PMID:6152665. S2CID:36099212. مؤرشف من الأصل في 2021-09-05.
Cosma MP، Pepe S، Annunziata I (مايو 2003). "The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases". Cell. ج. 113 ع. 4: 445–56. DOI:10.1016/S0092-8674(03)00348-9. PMID:12757706. S2CID:15095377.
Annunziata I، Bouchè V، Lombardi A (سبتمبر 2007). "Multiple sulfatase deficiency is due to hypomorphic mutations of the SUMF1 gene". Human Mutation. ج. 28 ع. 9: 298. DOI:10.1002/humu.9504. PMID:17657823. S2CID:8500605.
Dierks T، Schmidt B، Borissenko LV (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.
Preusser-Kunze A، Mariappan M، Schmidt B، Gande SL، Mutenda K، Wenzel D، von Figura K، Dierks T (أبريل 2005). "Molecular Characterization of the Human C(alpha)-formylglycine-generating Enzyme". Journal of Biological Chemistry. ج. 280 ع. 15: 14900–14910. DOI:10.1074/jbc.M413383200. PMID:15657036.
Landgrebe J، Dierks T، Schmidt B (أكتوبر 2003). "The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes". Gene. ج. 316: 47–56. DOI:10.1016/S0378-1119(03)00746-7. PMID:14563551. مؤرشف من الأصل في 2022-03-03.
Schlotawa، L؛ Adang، LA؛ Radhakrishnan، K؛ Ahrens-Nicklas، RC (13 مايو 2020). "Multiple sulfatase deficiency: A disease comprising mucopolysaccharidosis, sphingolipidosis, and more caused by a defect in posttranslational modification". International Journal of Molecular Sciences. ج. 21 ع. 10: 3448. DOI:10.3390/ijms21103448. PMC:7279497. PMID:32414121.

ncbi.nlm.nih.gov

Schlotawa، L؛ Adang، LA؛ Radhakrishnan، K؛ Ahrens-Nicklas، RC (13 مايو 2020). "Multiple sulfatase deficiency: A disease comprising mucopolysaccharidosis, sphingolipidosis, and more caused by a defect in posttranslational modification". International Journal of Molecular Sciences. ج. 21 ع. 10: 3448. DOI:10.3390/ijms21103448. PMC:7279497. PMID:32414121.

semanticscholar.org

api.semanticscholar.org

Dierks, T؛ Schmidt, B؛ Borissenko, Lv؛ Peng, J؛ Preusser, A؛ Mariappan, M؛ Von, Figura K (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.
Schmidt, B؛ Selmer, T؛ Ingendoh, A؛ Von, Figura K (يوليو 1995). "A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency". Cell. ج. 82 ع. 2: 271–8. DOI:10.1016/0092-8674(95)90314-3. PMID:7628016. S2CID:5864312.
Soong BW، Casamassima AC، Fink JK، Constantopoulos G، Horwitz AL (1988). "Multiple sulfatase deficiency". Neurology. ج. 38 ع. 8: 1273–5. DOI:10.1212/wnl.38.8.1273. PMID:2899861. S2CID:35222500.
Farooqui AA، Horrocks LA (1984). "Biochemical aspects of globoid and metachromatic leukodystrophies". Neurochem Pathol. ج. 2 ع. 3: 189–218. DOI:10.1007/BF02834352. PMID:6152665. S2CID:36099212. مؤرشف من الأصل في 2021-09-05.
Cosma MP، Pepe S، Annunziata I (مايو 2003). "The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases". Cell. ج. 113 ع. 4: 445–56. DOI:10.1016/S0092-8674(03)00348-9. PMID:12757706. S2CID:15095377.
Annunziata I، Bouchè V، Lombardi A (سبتمبر 2007). "Multiple sulfatase deficiency is due to hypomorphic mutations of the SUMF1 gene". Human Mutation. ج. 28 ع. 9: 298. DOI:10.1002/humu.9504. PMID:17657823. S2CID:8500605.
Dierks T، Schmidt B، Borissenko LV (مايو 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme". Cell. ج. 113 ع. 4: 435–44. DOI:10.1016/S0092-8674(03)00347-7. PMID:12757705. S2CID:11571659.

semanticscholar.org

Farooqui AA، Horrocks LA (1984). "Biochemical aspects of globoid and metachromatic leukodystrophies". Neurochem Pathol. ج. 2 ع. 3: 189–218. DOI:10.1007/BF02834352. PMID:6152665. S2CID:36099212. مؤرشف من الأصل في 2021-09-05.

thefreedictionary.com

medical-dictionary.thefreedictionary.com

The American Heritage Medical Dictionary: mucosulfatidosis نسخة محفوظة 2019-07-01 على موقع واي باك مشين.

web.archive.org

The American Heritage Medical Dictionary: mucosulfatidosis نسخة محفوظة 2019-07-01 على موقع واي باك مشين.
Farooqui AA، Horrocks LA (1984). "Biochemical aspects of globoid and metachromatic leukodystrophies". Neurochem Pathol. ج. 2 ع. 3: 189–218. DOI:10.1007/BF02834352. PMID:6152665. S2CID:36099212. مؤرشف من الأصل في 2021-09-05.
Landgrebe J، Dierks T، Schmidt B (أكتوبر 2003). "The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes". Gene. ج. 316: 47–56. DOI:10.1016/S0378-1119(03)00746-7. PMID:14563551. مؤرشف من الأصل في 2022-03-03.

wiley.com

onlinelibrary.wiley.com

Landgrebe J، Dierks T، Schmidt B (أكتوبر 2003). "The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes". Gene. ج. 316: 47–56. DOI:10.1016/S0378-1119(03)00746-7. PMID:14563551. مؤرشف من الأصل في 2022-03-03.