Safe stem cell treatment

A1 Medical Center is an experienced provider of tailored stem cell therapy. Since 2005, thousands of patients have been treated using our patented method in various clinics around the globe.

  • tailored
  • safe
  • proven
  • Neurological diseases
  • Autism
  • Lou Gehrig disease (ALS)
  • Arthritis
  • Spinal Cord Injury
  • Brain injury
  • Cerebral Palsy
  • Female Infertility
  • Male infertility
  • Parkinson
  • Heart Diseases
  • Eye diseases
  • Stroke
  • Multiple Sclerosis
  • Lung diseases like COPD
  • Sports Injuries 
diseases-treated

and also

1 Acatalasia/ Takahara’s disease

2 Activator Deficiency

3 Acute intermittent porphyria

4 Acyl-CoA oxidase deficiency

5 Addison disease

6 Adrenoleukodystrophy

7 Adult Refsum disease

8 Alexander disease

9 Alkaptonurira

10 Allan-Herndon-Dudley syndrome

11 5-alpha-reductase deficiency

12 Alpha-methylcayl-CoA racemase deficiency

13 Alpha-mannosidosis

14 Aminoacylase 1 deficiency

15 Amyloidosis

16 Amyotrophic lateral sclerosis

17 Andersen’s disease

18 Anoxic brain damage

19 Apparent mineralocorticoid excess syndrome

20 Argininemia

21 Argininosuccinic aciduria

22 Arnold-Chiari malformation outcomes

23 Aromatase deficiency

24 Aromatase excess syndrome

25 Arteriosclerosis

26 Aspartylglucosaminuria

27 Asperger syndrome

28 Asthma

29 Ataxia

30 Atherosclerosis

31 Atopic dermatitis, eczema

32 Atrophic gastritis

33 Atrophic vaginitis

34 Autism

35 Balint’s syndrome

36 Batten-Spielmeyer-Sjögren-Vogt

37 Behçet’s disease

38 Bernard-Soulier syndrome

39 Best’s Disease

40 Beta-mannosidosis

41 Betaketothiolase deficiency

42 Biotinidase deficiency

43 Brunner’s syndrome

44 Bullous emphysema

45 Bullous pemphigoid

46 Burns (Classic thermal and frostbite)

47 Canavan disease

48 Carbamoyl-phosphate synthase I deficiency

49 Cardiac insufficiency

50 Cardiomyopathy

51 Carnitine-acylcarnitine translocase deficiency

52 Carnitine palmitoyltransferase deficiency

53 Carnosenemia

54 Cerebral amyloid angiopathy

55 Cerebral palsy

56 Cerebrotendineous xanthomatosis

57 Cerebrovascular diseases

58 Charles Bonnet Syndrome

59 Chemotherapy side effects (post chemotherapy)

60 Childhood disintegrative disorder

61 Cholesteryl ester storage disease

62 Chondroplasias- maintenance therapy

63 Chronic Critical Limb Ischemia

64 Chronic Hexosaminidase A Deficiency

65 Citrullinemia

66 Coenzyme A dehydrogenase deficiency

67 Color blindness

68 Cone-rod dystrophy

69 Congenital adrenal hyperplasia

70 congenital dyserythropoietic anemia

71 Congenital erythropoietic porphyria

72 Congenital hemolytic anemia (nonspherocytic)

73 Congestive heart failure

74 Coronary artery diseases

75 Cortical visual impairment

76 Cori’s disease

77 Crigler-Najjar symdrome

78 Crohn’s diseases

79 Cystathioninuria

80 Cystic fibrosis

81 Cystinosis

82 D-bifunctional protein deficiency

83 Danon disease

84 Dehydroxyacetonephosphate acyltransferase def

85 Dementia

86 Dermatomyositis

87 Diabetes Mellitus type 1

88 Diabetes Mellitus type 2

89 Diabetic Neuropathy

90 Dienoyl-CoA reductase deficiency

91 Dopamine Beta hydroxylase deficiency

92 Dubin-Johnson syndrome

93 Enthesitis, chronic

94 Epilepsy

95 Erythropoetic porphyria

96 Ethylmalonic encephalopathy

97 Fabry disease

98 Factor V deficiency, Owren disease

99 Factor X deficiency/Amyloid purpura

100 Familial alpha-lipoprotein deficiency

101 Familial male-limited precocious puberty

102 Fanconi-Bickel’ syndrome

103 Fanconi syndrome/ Oculocerebrorenal syndrome

104 Farber disease

105 Follicle-stimulating hormone insensitivity

106 Forbes’ disease

107 Fructose intolerance

108 Fucosidosis

109 Fumarase deficiency

110 G6PD/ Favism

111 Galactosemia

112 Galactosialidosis

113 Gangliosidosis (GM1)

114 Gaucher Disease

115 Glucocorticoid remedial aldosteronism

116 Gonadotropin-releasing hormone insensitivity

117 Goodpasture’s syndrome

118 Glanzmann’s thrombasthenia

119 Glutaric acidemia

120 Glycogen storage disease

121 Gout, severe and recurrent cases

122 Hartnup disease

123 Hashimoto’s thyroiditis, refractory cases

124 Hawkinsinuria

125 Heart failure

126 Hemophilia

127 Hereditary CNS demyelinating disease

128 Hereditary coproporphyria

129 Hereditary Fructose intolerance

130 Hermansky–Pudlak syndrome

131 Hers’ disease

132 Hexosaminidase A Deficiency

133 Histidenemia

134 Homocystinuria

135 Huntington’s disease

136 Hunter syndrome

137 Hurler Syndrome

138 Hyaluronidase Deficiency

139 4-Hydroxy-butyric aciduria (SSADHD)

140 2-Hydroxy-glutaric aciduria

141 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

142 Hyperargininemia

143 Hyperargininuria

144 Hyperhomocysteinuria

145 Hyperlysinemias

146 Hypermethioninemia

147 Hyperoxaluria/ Bird’s disease

148 Hyperprolinemia

149 Hypertrophic emphysema

150 Hypertryptophanemia

151 Hyperurecemia

152 Hypervalenemia

153 Hypo-alpha-lipoproteinemia

154 Iminoglycinuria

155 Inborn errors of steroid metabolism

156 Infantile Free Sialic Acid Storage Disease

157 Infantile Refsum disease

158 Intractable wound healing

159 Interstitial lung disease

160 Ionizing radiation injury

161 Isobutyryl-CoA dehydrogenase deficiency

162 Isolated 17,20-lyase deficiency

163 Isovaleric acIdemia

164 Jansky-Bielschowsky disease

165 Joint regeneration

166 Juvenile arthritis

167 Juvenile Hexosaminidase A Deficiency

168 Kernicterus- Bilirubin encephalopathy

169 Krabbe disease

170 Kufs disease

171 Lactose intolerance

172 Leber’s congenital amaurosis

173 Lesch-Nyhan syndrome

174 Leukopdystrophies

175 Leukoencephalopathy

176 Leydig cell hypoplasia

177 Lipoid congenital adrenal hyperplasia

178 Liver cirrhosis

179 Locked-in syndrome

180 Lysinuric protein intolerance

181 Lysosomal storage disease

182 Lysosomal acid lipase deficiency

183 Macular Degeneration

184 Malonyl-CoA decarboxylase deficiency

185 Mannosidosis

186 Maple syrup urine disease

187 Maroteaux-Lamy syndrome

188 Menkes disease

189 Metachromatic Leukodystrophy

190 3-Methylcrotonyl-CoA carboxylase deficiency

191 3-Methylglutaconic aciduria 1

192 Mevalonate kinase deficiency/aciduria

193 2-methylbutyryl CoA deficiency

194 Methylmalonic acidemia

195 Methylmalonyl-CoA mutase deficiency

196 Mitochondrial trifunctional protein deficiency

197 Morquio syndrome

198 Mucolipidosis (all types)

199 Mucopolysaccharidoses disorders

200 Mulibrey nanism

201 Multiple Sclerosis

202 Multiple sulfatase deficiency

203 Multiple system atrophy

204 Muscular dystrophy

205 Myelopathy

206 Myotonia congenita

207 Narcolepsy/cataplexy

208 N-Acetylglutamate synthase deficiency

209 Neonatal adrenoleukodystrophy

210 Nephropathy/Glomeronephritis

211 Neurological Visual Impairment

212 Neuromyelitis optica

213 Neuronal Ceroid Lipofuscinoses

214 Niemann-Pick Disease

215 Nonketotic hyperglycinemia

216 Northern Epilepsy syndrome

217 Obstructive lung disease

218 Ocular albinism

219 Optic Nerve Hypoplasia

220 Ornithine carbamoyltransferase deficiency

221 Osteomyelitis

222 Parkinson’s disease

223 Pemphigus

224 Pelizaeus–Merzbacher disease

225 Peripheral arterial diseases

226 Periventricular leukomalacia

227 Peroxisomal disorder

228 Peroxisome biogenesis disorders

229 Pervasive developmental disorder

230 Phenylketonuria

231 Pipecolic acedemia/ Hyperpipecolatemia

232 Polymyositis

233 Pompe’s disease

234 Porphyria cutanea tarda

235 Porphobilinogen synthase Deficiency

236 Primary biliary cirrhosis

237 Primary carnitine deficiency

238 Progressive supranuclear palsy

239 Prolidase deficiency

240 Propionic acidemia

241 Pseudo-Hurler polydystrophy

242 Psoriasis

243 Psoriatic arthritis

244 Pulmonary diseases

245 Pycnodysostosis

246 6-Pyruvoyltetrahydropterin synthase deficiency

247 Radiation injuries (Post radiation injuries)

248 Radiation induced lung injury

249 Reactive arthritis, Reiter’s sd

250 Red cell aldolase deficiency

251 Refsum disease

252 Reiter’s syndrome

253 Restrictive lung disease

254 Retinitis Pigmentosa

255 Retinopathy

256 Rett syndrome

257 Rheumatism

258 Rheumatoid arthritis

259 Rhizomelic chondrodysplasia punctata

260 Rotor syndrome

261 Saccharopinuria

262 Salla disease

263 Sandhoff disease

264 Sanfilippo syndrome

265 Santavuori-Haltia syndrome

266 Scheie Syndrome

267 Schindler disease

268 Scleroderma

269 Sialidosis

270 Sideroblastic anemia

271 Sjögren syndrome

272 Sly Syndrome

273 Spastic diplegia

274 Spinal Muscular Atrophy

275 Stargardt’s Disease

276 Sturge-Weber Syndrome

277 Stroke

278 Systemic lupus erythematosus

279 Tangier disease

280 Tarui’s disease

281 Tay-Sachs disease

282 Tetrahydrobiopterin deficiency

283 Thermal radiation injury

284 Trimethylaminuria/ fish odor syndrome

285 Tyrosinemia

286 Ulcerative Colititis

287 Urocanic aciduria

288 Usher Syndrome

289 Variegate porphyria

290 Vitelliform macular dystrophy

291 Vitiligo

292 Von Gierke’s disease

293 Von Willebrand disease

294 Waardenburg syndrome

295 Werdnig-Hoffman disease (SMA)

296 Wilson’s disease

297 Wolman disease

298 X-linked adrenoleukodystrophy

299 Zellweger syndrome

 

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