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Journal of the Turkish German Gynecology Association, ISSN 1309-0399, 2013, Volume 14, Issue 2, pp. 81 - 86
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 09/2015, Volume 373, Issue 11, pp. 1010 - 1020
Journal Article
The Journal of Pediatrics, ISSN 0022-3476, 01/2011, Volume 158, Issue 1, pp. 172 - 173
Journal Article
Journal of Pediatrics, ISSN 0022-3476, 01/2011, Volume 158, Issue 1, pp. 172 - 173
Journal Article
The Journal of Pediatrics, ISSN 0022-3476, 2011, Volume 158, Issue 1, pp. 172 - 173
Journal Article
JOURNAL OF PEDIATRICS, ISSN 0022-3476, 01/2011, Volume 158, Issue 1, pp. 172 - 173
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 6, pp. 533 - 542
Journal Article
Therapeutics and Clinical Risk Management, ISSN 1176-6336, 2008, Volume 4, Issue 2, pp. 425 - 431
Journal Article
Dermatologic Therapy, ISSN 1396-0296, 07/2019, Volume 32, Issue 4, pp. e12927 - n/a
Linear IgA dermatosis (LAD) is a rare, subepidermal blistering disease with mucocutaneous involvement. It may be idiopathic or drug induced. We describe a... 
linear IgA dermatosis | cefixime | drug eruption | bullous | childhood | DISEASE | BULLOUS DERMATOSIS | DERMATOLOGY | Moxalactam | Cephaloridine | Urinary tract infections | Cephalosporins | Immunoglobulin A | Index Medicus
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 08/2019, Volume 14, Issue 1, pp. 198 - 198
Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive disorder that can present as a severe, infantile form also known as Wolman disease. We... 
Wolman disease | WOLMAN-DISEASE | MEDICINE, RESEARCH & EXPERIMENTAL | SPLEEN | Adrenal insufficiency | Diet | Enzyme replacement therapy | Lysosomal acid lipase deficiency | GENETICS & HEREDITY | CELL TRANSPLANTATION | Infants (Newborn) | Enzymes | Care and treatment | Triglycerides | Infants | Hypothyroidism | Lipase | Cardiology | Health aspects | Diseases | Index Medicus
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 01/2019, Volume 42, Issue 1, pp. 140 - 146
BackgroundGlutamate formiminotransferase deficiency (FTCD deficiency) or formiminoglutamic aciduria is the second most common of the known inherited disorders... 
MEDICINE, RESEARCH & EXPERIMENTAL | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | FORMIMINOTRANSFERASE-DEFICIENCY SYNDROME | Phenotypes | Anemia | Intellectual disabilities | Case reports | Glutamate formiminotransferase | Aciduria | Mass spectroscopy | Infants | Medical screening | Folic acid | Hereditary diseases | Index Medicus
Journal Article
Journal Article
FERTILITY AND STERILITY, ISSN 0015-0282, 03/2006, Volume 85, Issue 3, pp. 592 - 596
Objective: To determine the predictive value of antimullerian hormone (AMH) as a marker for ovarian reserve and to compare its value with the markers currently... 
TESTS | MULLERIAN-INHIBITING SUBSTANCE | VOLUME | PREDICTIVE-VALUE | ovarian reserve | OBSTETRICS & GYNECOLOGY | TRANSVAGINAL SONOGRAPHY | REPRODUCTIVE BIOLOGY | serum antimullerian hormone (AMH) | CYCLES | IVF | IN-VITRO FERTILIZATION | REPRODUCTIVE AGE | DAY-3
Journal Article
Pediatrics, ISSN 0031-4005, 09/2009, Volume 124, Issue 3, pp. 972 - 979
Journal Article
Fertility and Sterility, ISSN 0015-0282, 2015, Volume 104, Issue 3, pp. e255 - e255
Journal Article
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