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Annals of Saudi Medicine, ISSN 0256-4947, 05/2017, Volume 37, Issue 3, pp. 212 - 215
Journal Article
Canadian Family Physician, ISSN 0008-350X, 7/2013, Volume 59, Issue 7, pp. 748 - 748
Journal Article
Canadian Family Physician, ISSN 0008-350X, 7/2013, Volume 59, Issue 7, pp. 750 - 751
Journal Article
Canadian Family Physician, ISSN 0008-350X, 3/2013, Volume 59, Issue 3, pp. 272 - 272
Journal Article
Canadian Family Physician, ISSN 0008-350X, 3/2013, Volume 59, Issue 3, pp. 271 - 271
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 05/2015, Volume 35, Issue 3, pp. 254 - 256
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 01/2018, Volume 38, Issue 1, pp. 522 - 525
BACKGROUND: Skin cancer is the most common cancer worldwide; one in every three diagnosed malignancies is a skin cancer. However, skin cancer is rarely... 
MEDICINE, GENERAL & INTERNAL | PATTERN | BASAL-CELL CARCINOMA | REGION | Health risk assessment | Age | Skin cancer | Original
Journal Article
CANADIAN FAMILY PHYSICIAN, ISSN 0008-350X, 07/2013, Volume 59, Issue 7, pp. 748 - 748
Journal Article
CANADIAN FAMILY PHYSICIAN, ISSN 0008-350X, 03/2013, Volume 59, Issue 3, pp. 271 - 272
Journal Article
Canadian family physician Medecin de famille canadien, 03/2013, Volume 59, Issue 3, p. 271
Journal Article
Journal Medical Libanais, ISSN 0023-9852, 2018, Volume 66, Issue 3, pp. 170 - 172
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 07/2017, Volume 34, Issue 4, pp. 461 - 464
Background/Objectives Many dermatologic and systemic diseases have been reported in association with hidradenitis suppurativa, but its association with Down... 
PATHOGENESIS | PEDIATRICS | GLANDS | APOCRINE | DISEASE | DERMATOLOGY | Young Adult | Hidradenitis Suppurativa - epidemiology | Prospective Studies | Humans | Adolescent | Down Syndrome - complications | Adult | Female | Male | Saudi Arabia - epidemiology | Hidradenitis Suppurativa - complications | Medicine, Experimental | Medical research | Down syndrome | Down's syndrome
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 11/2010, Volume 30, Issue 6, pp. 499 - 499
  A 27-year-old woman, 28-weeks pregnant, presented with a rapidly growing nodule on her finger with spontaneous bleeding over the previous 4 weeks. Physical... 
MEDICINE, GENERAL & INTERNAL | Pregnancy | Diagnosis, Differential | Humans | Neoplasms, Vascular Tissue - pathology | Adult | Female | Fingers - pathology | Granuloma, Pyogenic - pathology | Case studies | Cautery | Usage | Cardiovascular tumors | Pregnant women | Fingers | Melanoma | Diagnosis | Health aspects | Diseases | Medical diagnosis | Fingers & toes | Skin cancer | Tumors | What's Your Diagnosis?
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 01/2019, Volume 39, Issue 1, p. 56
D-penicillamine (DPA)-induced pseudo-pseudoxanthoma elasticum (PXE) and elastosis perforans serpiginosa (EPS) has been reported in the past, but most of the... 
Family medical history | Psoriasis | Dermatology | Biopsy | Research centers | Drug dosages
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2017, Volume 173, Issue 4, pp. 1009 - 1016
Hereditary sensory autonomic neuropathy type IV (HSAN‐IV) is a rare autosomal recessive disorder that usually begins in infancy and is characterized by... 
NGF‐nerve growth factor | ADHD‐attention deficit hyperactivity disorder | CIPA‐congenital insensitivity to pain with anhidrosis | NTRK1‐neurotrophic tyrosine kinase receptor type 1 | HSAN‐hereditary sensory and autonomic neuropathy | NGF-nerve growth factor | CIPA-congenital insensitivity to pain with anhidrosis | ADHD-attention deficit hyperactivity disorder | NTRK1-neurotrophic tyrosine kinase receptor type 1 | HSAN-hereditary sensory and autonomic neuropathy | CONGENITAL INSENSITIVITY | TYROSINE KINASE | TRKA/NGF RECEPTOR GENE | NERVE GROWTH-FACTOR | HIGH-AFFINITY RECEPTOR | ANHIDROSIS CIPA | PAIN | GENETICS & HEREDITY | TRK RECEPTORS | NEUROTROPHIN RECEPTORS | NEUROPATHY TYPE-IV | Neurons - pathology | Hereditary Sensory and Autonomic Neuropathies - physiopathology | Humans | Child, Preschool | Male | Mutation, Missense | Exome | Saudi Arabia | Chromosomes, Human, Pair 1 | Base Sequence | Female | Neurons - metabolism | Child | Hypohidrosis - physiopathology | Severity of Illness Index | Gene Expression | Nerve Growth Factor - metabolism | Protein Structure, Secondary | Models, Molecular | Nerve Growth Factor - genetics | Codon, Nonsense | Genes, Recessive | Intellectual Disability - physiopathology | Phenotype | Self-Injurious Behavior - physiopathology | Receptor, trkA - metabolism | Adolescent | Receptor, trkA - chemistry | Protein Binding | Receptor, trkA - genetics | Hereditary Sensory and Autonomic Neuropathies - genetics | Consanguinity | High-Throughput Nucleotide Sequencing | Hereditary Sensory and Autonomic Neuropathies - diagnosis | Tyrosine | Nerve growth factor | Genetic aspects | Genotype & phenotype | Rodents | Mutation
Journal Article
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